Canonical Allele Identifier: CA351204731

Gene: LRRFIP1

Linked Data

• MyVariant Identifiers: chr2:g.238672574G>T (hg19) ; chr2:g.237763931G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237763931G>T , CM000664.2:g.237763931G>T	GRCh38
NC_000002.11:g.238672574G>T , CM000664.1:g.238672574G>T	GRCh37
NC_000002.10:g.238337313G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698097.1:c.1181+3726G>T
ENST00000698098.1:c.955+3726G>T	ENSP00000513562.1:n.955+3726G>T
ENST00000308482.14:c.1459+3726G>T MANE Select	ENSP00000310109.9:n.1459+3726G>T
ENST00000244815.9:c.2146G>T	ENSP00000244815.5:p.Asp716Tyr
ENST00000289175.10:c.2050G>T	ENSP00000289175.6:p.Asp684Tyr
ENST00000308482.13:c.1459+3726G>T	ENSP00000310109.9:n.1459+3726G>T
ENST00000392000.4:c.2218G>T	ENSP00000375857.4:p.Asp740Tyr
ENST00000483443.1:n.235+3726G>T
NM_001137550.1:c.1459+3726G>T	NP_001131022.1:n.1459+3726G>T
NM_001137551.1:c.721+3726G>T	NP_001131023.1:n.721+3726G>T
NM_001137552.1:c.2218G>T	NP_001131024.1:p.Asp740Tyr
NM_001137553.1:c.2050G>T	NP_001131025.1:p.Asp684Tyr
NM_004735.3:c.2146G>T	NP_004726.2:p.Asp716Tyr
XM_005246112.3:c.2851G>T	XP_005246169.1:p.Asp951Tyr
XM_005246115.3:c.2806G>T	XP_005246172.1:p.Asp936Tyr
XM_005246116.3:c.2788G>T	XP_005246173.1:p.Asp930Tyr
XM_005246118.3:c.2743G>T	XP_005246175.1:p.Asp915Tyr
XM_005246119.3:c.2740G>T	XP_005246176.1:p.Asp914Tyr
XM_005246120.3:c.2704G>T	XP_005246177.1:p.Asp902Tyr
XM_005246121.3:c.2689G>T	XP_005246178.1:p.Asp897Tyr
XM_005246122.3:c.2677G>T	XP_005246179.1:p.Asp893Tyr
XM_005246124.1:c.2659G>T	XP_005246181.1:p.Asp887Tyr
XM_005246125.3:c.2638G>T	XP_005246182.1:p.Asp880Tyr
XM_005246126.3:c.2599G>T	XP_005246183.1:p.Asp867Tyr
XM_005246128.1:c.2566G>T	XP_005246185.1:p.Asp856Tyr
XM_005246129.3:c.2527G>T	XP_005246186.1:p.Asp843Tyr
XM_005246130.3:c.2500G>T	XP_005246187.1:p.Asp834Tyr
XM_005246131.3:c.2413G>T	XP_005246188.1:p.Asp805Tyr
XM_005246132.3:c.2338G>T	XP_005246189.1:p.Asp780Tyr
XM_005246133.1:c.2308G>T	XP_005246190.1:p.Asp770Tyr
XM_005246134.1:c.2266G>T	XP_005246191.1:p.Asp756Tyr
XM_005246135.1:c.2236G>T	XP_005246192.1:p.Asp746Tyr
XM_005246136.1:c.2080G>T	XP_005246193.1:p.Asp694Tyr
XM_005246141.3:c.823+3726G>T	XP_005246198.1:n.823+3726G>T
XM_005246142.1:c.751+3726G>T	XP_005246199.1:n.751+3726G>T
XM_006712842.2:c.2749G>T	XP_006712905.1:p.Asp917Tyr
XM_006712843.2:c.2644G>T	XP_006712906.1:p.Asp882Tyr
XM_006712844.1:c.2578G>T	XP_006712907.1:p.Asp860Tyr
XM_006712845.2:c.2560G>T	XP_006712908.1:p.Asp854Tyr
XM_006712846.1:c.2464G>T	XP_006712909.1:p.Asp822Tyr
XM_006712847.1:c.2404G>T	XP_006712910.1:p.Asp802Tyr
XM_006712848.1:c.2332G>T	XP_006712911.1:p.Asp778Tyr
XM_011512152.1:c.2884G>T	XP_011510454.1:p.Asp962Tyr
XM_011512153.1:c.2866G>T	XP_011510455.1:p.Asp956Tyr
XM_011512154.1:c.2854G>T	XP_011510456.1:p.Asp952Tyr
XM_011512155.1:c.2845G>T	XP_011510457.1:p.Asp949Tyr
XM_011512156.1:c.2812G>T	XP_011510458.1:p.Asp938Tyr
XM_011512157.1:c.2698G>T	XP_011510459.1:p.Asp900Tyr
XM_011512158.1:c.2626G>T	XP_011510460.1:p.Asp876Tyr
XM_011512159.1:c.2434G>T	XP_011510461.1:p.Asp812Tyr
XM_011512160.1:c.1555+3726G>T	XP_011510462.1:n.1555+3726G>T
XM_011512161.1:c.1555+3726G>T	XP_011510463.1:n.1555+3726G>T
XM_011512162.1:c.1369+3726G>T	XP_011510464.1:n.1369+3726G>T
XM_011512163.1:c.1297+3726G>T	XP_011510465.1:n.1297+3726G>T
XM_011512164.1:c.751+3726G>T	XP_011510466.1:n.751+3726G>T
XM_011512165.1:c.721+3726G>T	XP_011510467.1:n.721+3726G>T
XM_011512166.1:c.1516+3726G>T	XP_011510468.1:n.1516+3726G>T
XR_923063.1:n.1605+3726G>T
XM_005246141.4:c.823+3726G>T	XP_005246198.1:n.823+3726G>T
XM_005246142.2:c.751+3726G>T	XP_005246199.1:n.751+3726G>T
XM_017005253.2:c.1522+3726G>T	XP_016860742.1:n.1522+3726G>T
XM_017005254.2:c.1522+3726G>T	XP_016860743.1:n.1522+3726G>T
XM_017005255.2:c.1450+3726G>T	XP_016860744.1:n.1450+3726G>T
XM_017005256.2:c.1336+3726G>T	XP_016860745.1:n.1336+3726G>T
XM_017005257.2:c.1387+3726G>T	XP_016860746.1:n.1387+3726G>T
XM_017005258.2:c.1336+3726G>T	XP_016860747.1:n.1336+3726G>T
XM_017005260.2:c.1162+3726G>T	XP_016860749.1:n.1162+3726G>T
XM_017005261.2:c.1099+3726G>T	XP_016860750.1:n.1099+3726G>T
XM_017005262.2:c.1099+3726G>T	XP_016860751.1:n.1099+3726G>T
XM_017005263.2:c.937+3726G>T	XP_016860752.1:n.937+3726G>T
XR_001739039.2:n.2920G>T
XR_001739040.1:n.3085G>T
XR_001739041.2:n.2881G>T
XR_001739042.2:n.2857G>T
XR_001739043.1:n.2833G>T
XR_001739044.2:n.2848G>T
XR_001739045.2:n.2818G>T
XR_001739046.1:n.3165G>T
XR_001739047.2:n.2734G>T
XR_001739048.1:n.2923G>T
XR_001739049.2:n.2668G>T
XR_001739050.2:n.2629G>T
XR_001739051.2:n.2596G>T
XR_001739052.2:n.2569G>T
XR_001739053.1:n.2558G>T
XR_001739054.1:n.2480G>T
XR_001739055.2:n.2497G>T
XR_001739056.2:n.2482G>T
XR_001739057.1:n.2498G>T
XR_001739058.1:n.2677G>T
XR_001739059.2:n.2410G>T
XR_001739060.1:n.2384G>T
XR_001739061.1:n.2426G>T
XR_001739062.1:n.2603G>T
XR_001739063.1:n.2310G>T
XR_001739064.1:n.2571G>T
XR_001739065.1:n.2515G>T
XR_001739066.1:n.2312G>T
XR_001739067.1:n.2219G>T
XR_001739068.1:n.2240G>T
XR_001739069.1:n.2417G>T
XR_001739070.1:n.2281G>T
XR_001739071.1:n.2139G>T
XR_001739072.1:n.2385G>T
XR_001739073.2:n.1591+3726G>T
XR_002959364.1:n.2311G>T
NM_001137550.2:c.1459+3726G>T MANE Select	NP_001131022.1:n.1459+3726G>T
NM_001137552.2:c.2218G>T	NP_001131024.1:p.Asp740Tyr
NM_001137553.2:c.2050G>T	NP_001131025.1:p.Asp684Tyr
NM_004735.4:c.2146G>T	NP_004726.2:p.Asp716Tyr
NM_001137551.2:c.721+3726G>T	NP_001131023.1:n.721+3726G>T