Canonical Allele Identifier: CA351204567

Gene: LRRFIP1

Linked Data

• dbSNP Id: rs2150875184
• MyVariant Identifiers: chr2:g.238672535A>T (hg19) ; chr2:g.237763892A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237763892A>T , CM000664.2:g.237763892A>T	GRCh38
NC_000002.11:g.238672535A>T , CM000664.1:g.238672535A>T	GRCh37
NC_000002.10:g.238337274A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698097.1:c.1181+3687A>T
ENST00000698098.1:c.955+3687A>T	ENSP00000513562.1:n.955+3687A>T
ENST00000308482.14:c.1459+3687A>T MANE Select	ENSP00000310109.9:n.1459+3687A>T
ENST00000244815.9:c.2107A>T	ENSP00000244815.5:p.Thr703Ser
ENST00000289175.10:c.2011A>T	ENSP00000289175.6:p.Thr671Ser
ENST00000308482.13:c.1459+3687A>T	ENSP00000310109.9:n.1459+3687A>T
ENST00000392000.4:c.2179A>T	ENSP00000375857.4:p.Thr727Ser
ENST00000483443.1:n.235+3687A>T
NM_001137550.1:c.1459+3687A>T	NP_001131022.1:n.1459+3687A>T
NM_001137551.1:c.721+3687A>T	NP_001131023.1:n.721+3687A>T
NM_001137552.1:c.2179A>T	NP_001131024.1:p.Thr727Ser
NM_001137553.1:c.2011A>T	NP_001131025.1:p.Thr671Ser
NM_004735.3:c.2107A>T	NP_004726.2:p.Thr703Ser
XM_005246112.3:c.2812A>T	XP_005246169.1:p.Thr938Ser
XM_005246115.3:c.2767A>T	XP_005246172.1:p.Thr923Ser
XM_005246116.3:c.2749A>T	XP_005246173.1:p.Thr917Ser
XM_005246118.3:c.2704A>T	XP_005246175.1:p.Thr902Ser
XM_005246119.3:c.2701A>T	XP_005246176.1:p.Thr901Ser
XM_005246120.3:c.2665A>T	XP_005246177.1:p.Thr889Ser
XM_005246121.3:c.2650A>T	XP_005246178.1:p.Thr884Ser
XM_005246122.3:c.2638A>T	XP_005246179.1:p.Thr880Ser
XM_005246124.1:c.2620A>T	XP_005246181.1:p.Thr874Ser
XM_005246125.3:c.2599A>T	XP_005246182.1:p.Thr867Ser
XM_005246126.3:c.2560A>T	XP_005246183.1:p.Thr854Ser
XM_005246128.1:c.2527A>T	XP_005246185.1:p.Thr843Ser
XM_005246129.3:c.2488A>T	XP_005246186.1:p.Thr830Ser
XM_005246130.3:c.2461A>T	XP_005246187.1:p.Thr821Ser
XM_005246131.3:c.2374A>T	XP_005246188.1:p.Thr792Ser
XM_005246132.3:c.2299A>T	XP_005246189.1:p.Thr767Ser
XM_005246133.1:c.2269A>T	XP_005246190.1:p.Thr757Ser
XM_005246134.1:c.2227A>T	XP_005246191.1:p.Thr743Ser
XM_005246135.1:c.2197A>T	XP_005246192.1:p.Thr733Ser
XM_005246136.1:c.2041A>T	XP_005246193.1:p.Thr681Ser
XM_005246141.3:c.823+3687A>T	XP_005246198.1:n.823+3687A>T
XM_005246142.1:c.751+3687A>T	XP_005246199.1:n.751+3687A>T
XM_006712842.2:c.2710A>T	XP_006712905.1:p.Thr904Ser
XM_006712843.2:c.2605A>T	XP_006712906.1:p.Thr869Ser
XM_006712844.1:c.2539A>T	XP_006712907.1:p.Thr847Ser
XM_006712845.2:c.2521A>T	XP_006712908.1:p.Thr841Ser
XM_006712846.1:c.2425A>T	XP_006712909.1:p.Thr809Ser
XM_006712847.1:c.2365A>T	XP_006712910.1:p.Thr789Ser
XM_006712848.1:c.2293A>T	XP_006712911.1:p.Thr765Ser
XM_011512152.1:c.2845A>T	XP_011510454.1:p.Thr949Ser
XM_011512153.1:c.2827A>T	XP_011510455.1:p.Thr943Ser
XM_011512154.1:c.2815A>T	XP_011510456.1:p.Thr939Ser
XM_011512155.1:c.2806A>T	XP_011510457.1:p.Thr936Ser
XM_011512156.1:c.2773A>T	XP_011510458.1:p.Thr925Ser
XM_011512157.1:c.2659A>T	XP_011510459.1:p.Thr887Ser
XM_011512158.1:c.2587A>T	XP_011510460.1:p.Thr863Ser
XM_011512159.1:c.2395A>T	XP_011510461.1:p.Thr799Ser
XM_011512160.1:c.1555+3687A>T	XP_011510462.1:n.1555+3687A>T
XM_011512161.1:c.1555+3687A>T	XP_011510463.1:n.1555+3687A>T
XM_011512162.1:c.1369+3687A>T	XP_011510464.1:n.1369+3687A>T
XM_011512163.1:c.1297+3687A>T	XP_011510465.1:n.1297+3687A>T
XM_011512164.1:c.751+3687A>T	XP_011510466.1:n.751+3687A>T
XM_011512165.1:c.721+3687A>T	XP_011510467.1:n.721+3687A>T
XM_011512166.1:c.1516+3687A>T	XP_011510468.1:n.1516+3687A>T
XR_923063.1:n.1605+3687A>T
XM_005246141.4:c.823+3687A>T	XP_005246198.1:n.823+3687A>T
XM_005246142.2:c.751+3687A>T	XP_005246199.1:n.751+3687A>T
XM_017005253.2:c.1522+3687A>T	XP_016860742.1:n.1522+3687A>T
XM_017005254.2:c.1522+3687A>T	XP_016860743.1:n.1522+3687A>T
XM_017005255.2:c.1450+3687A>T	XP_016860744.1:n.1450+3687A>T
XM_017005256.2:c.1336+3687A>T	XP_016860745.1:n.1336+3687A>T
XM_017005257.2:c.1387+3687A>T	XP_016860746.1:n.1387+3687A>T
XM_017005258.2:c.1336+3687A>T	XP_016860747.1:n.1336+3687A>T
XM_017005260.2:c.1162+3687A>T	XP_016860749.1:n.1162+3687A>T
XM_017005261.2:c.1099+3687A>T	XP_016860750.1:n.1099+3687A>T
XM_017005262.2:c.1099+3687A>T	XP_016860751.1:n.1099+3687A>T
XM_017005263.2:c.937+3687A>T	XP_016860752.1:n.937+3687A>T
XR_001739039.2:n.2881A>T
XR_001739040.1:n.3046A>T
XR_001739041.2:n.2842A>T
XR_001739042.2:n.2818A>T
XR_001739043.1:n.2794A>T
XR_001739044.2:n.2809A>T
XR_001739045.2:n.2779A>T
XR_001739046.1:n.3126A>T
XR_001739047.2:n.2695A>T
XR_001739048.1:n.2884A>T
XR_001739049.2:n.2629A>T
XR_001739050.2:n.2590A>T
XR_001739051.2:n.2557A>T
XR_001739052.2:n.2530A>T
XR_001739053.1:n.2519A>T
XR_001739054.1:n.2441A>T
XR_001739055.2:n.2458A>T
XR_001739056.2:n.2443A>T
XR_001739057.1:n.2459A>T
XR_001739058.1:n.2638A>T
XR_001739059.2:n.2371A>T
XR_001739060.1:n.2345A>T
XR_001739061.1:n.2387A>T
XR_001739062.1:n.2564A>T
XR_001739063.1:n.2271A>T
XR_001739064.1:n.2532A>T
XR_001739065.1:n.2476A>T
XR_001739066.1:n.2273A>T
XR_001739067.1:n.2180A>T
XR_001739068.1:n.2201A>T
XR_001739069.1:n.2378A>T
XR_001739070.1:n.2242A>T
XR_001739071.1:n.2100A>T
XR_001739072.1:n.2346A>T
XR_001739073.2:n.1591+3687A>T
XR_002959364.1:n.2272A>T
NM_001137550.2:c.1459+3687A>T MANE Select	NP_001131022.1:n.1459+3687A>T
NM_001137552.2:c.2179A>T	NP_001131024.1:p.Thr727Ser
NM_001137553.2:c.2011A>T	NP_001131025.1:p.Thr671Ser
NM_004735.4:c.2107A>T	NP_004726.2:p.Thr703Ser
NM_001137551.2:c.721+3687A>T	NP_001131023.1:n.721+3687A>T