Canonical Allele Identifier: CA351204560

Gene: LRRFIP1

Linked Data

• MyVariant Identifiers: chr2:g.238672534C>G (hg19) ; chr2:g.237763891C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237763891C>G , CM000664.2:g.237763891C>G	GRCh38
NC_000002.11:g.238672534C>G , CM000664.1:g.238672534C>G	GRCh37
NC_000002.10:g.238337273C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698097.1:c.1181+3686C>G
ENST00000698098.1:c.955+3686C>G	ENSP00000513562.1:n.955+3686C>G
ENST00000308482.14:c.1459+3686C>G MANE Select	ENSP00000310109.9:n.1459+3686C>G
ENST00000244815.9:c.2106C>G	ENSP00000244815.5:p.Cys702Trp
ENST00000289175.10:c.2010C>G	ENSP00000289175.6:p.Cys670Trp
ENST00000308482.13:c.1459+3686C>G	ENSP00000310109.9:n.1459+3686C>G
ENST00000392000.4:c.2178C>G	ENSP00000375857.4:p.Cys726Trp
ENST00000483443.1:n.235+3686C>G
NM_001137550.1:c.1459+3686C>G	NP_001131022.1:n.1459+3686C>G
NM_001137551.1:c.721+3686C>G	NP_001131023.1:n.721+3686C>G
NM_001137552.1:c.2178C>G	NP_001131024.1:p.Cys726Trp
NM_001137553.1:c.2010C>G	NP_001131025.1:p.Cys670Trp
NM_004735.3:c.2106C>G	NP_004726.2:p.Cys702Trp
XM_005246112.3:c.2811C>G	XP_005246169.1:p.Cys937Trp
XM_005246115.3:c.2766C>G	XP_005246172.1:p.Cys922Trp
XM_005246116.3:c.2748C>G	XP_005246173.1:p.Cys916Trp
XM_005246118.3:c.2703C>G	XP_005246175.1:p.Cys901Trp
XM_005246119.3:c.2700C>G	XP_005246176.1:p.Cys900Trp
XM_005246120.3:c.2664C>G	XP_005246177.1:p.Cys888Trp
XM_005246121.3:c.2649C>G	XP_005246178.1:p.Cys883Trp
XM_005246122.3:c.2637C>G	XP_005246179.1:p.Cys879Trp
XM_005246124.1:c.2619C>G	XP_005246181.1:p.Cys873Trp
XM_005246125.3:c.2598C>G	XP_005246182.1:p.Cys866Trp
XM_005246126.3:c.2559C>G	XP_005246183.1:p.Cys853Trp
XM_005246128.1:c.2526C>G	XP_005246185.1:p.Cys842Trp
XM_005246129.3:c.2487C>G	XP_005246186.1:p.Cys829Trp
XM_005246130.3:c.2460C>G	XP_005246187.1:p.Cys820Trp
XM_005246131.3:c.2373C>G	XP_005246188.1:p.Cys791Trp
XM_005246132.3:c.2298C>G	XP_005246189.1:p.Cys766Trp
XM_005246133.1:c.2268C>G	XP_005246190.1:p.Cys756Trp
XM_005246134.1:c.2226C>G	XP_005246191.1:p.Cys742Trp
XM_005246135.1:c.2196C>G	XP_005246192.1:p.Cys732Trp
XM_005246136.1:c.2040C>G	XP_005246193.1:p.Cys680Trp
XM_005246141.3:c.823+3686C>G	XP_005246198.1:n.823+3686C>G
XM_005246142.1:c.751+3686C>G	XP_005246199.1:n.751+3686C>G
XM_006712842.2:c.2709C>G	XP_006712905.1:p.Cys903Trp
XM_006712843.2:c.2604C>G	XP_006712906.1:p.Cys868Trp
XM_006712844.1:c.2538C>G	XP_006712907.1:p.Cys846Trp
XM_006712845.2:c.2520C>G	XP_006712908.1:p.Cys840Trp
XM_006712846.1:c.2424C>G	XP_006712909.1:p.Cys808Trp
XM_006712847.1:c.2364C>G	XP_006712910.1:p.Cys788Trp
XM_006712848.1:c.2292C>G	XP_006712911.1:p.Cys764Trp
XM_011512152.1:c.2844C>G	XP_011510454.1:p.Cys948Trp
XM_011512153.1:c.2826C>G	XP_011510455.1:p.Cys942Trp
XM_011512154.1:c.2814C>G	XP_011510456.1:p.Cys938Trp
XM_011512155.1:c.2805C>G	XP_011510457.1:p.Cys935Trp
XM_011512156.1:c.2772C>G	XP_011510458.1:p.Cys924Trp
XM_011512157.1:c.2658C>G	XP_011510459.1:p.Cys886Trp
XM_011512158.1:c.2586C>G	XP_011510460.1:p.Cys862Trp
XM_011512159.1:c.2394C>G	XP_011510461.1:p.Cys798Trp
XM_011512160.1:c.1555+3686C>G	XP_011510462.1:n.1555+3686C>G
XM_011512161.1:c.1555+3686C>G	XP_011510463.1:n.1555+3686C>G
XM_011512162.1:c.1369+3686C>G	XP_011510464.1:n.1369+3686C>G
XM_011512163.1:c.1297+3686C>G	XP_011510465.1:n.1297+3686C>G
XM_011512164.1:c.751+3686C>G	XP_011510466.1:n.751+3686C>G
XM_011512165.1:c.721+3686C>G	XP_011510467.1:n.721+3686C>G
XM_011512166.1:c.1516+3686C>G	XP_011510468.1:n.1516+3686C>G
XR_923063.1:n.1605+3686C>G
XM_005246141.4:c.823+3686C>G	XP_005246198.1:n.823+3686C>G
XM_005246142.2:c.751+3686C>G	XP_005246199.1:n.751+3686C>G
XM_017005253.2:c.1522+3686C>G	XP_016860742.1:n.1522+3686C>G
XM_017005254.2:c.1522+3686C>G	XP_016860743.1:n.1522+3686C>G
XM_017005255.2:c.1450+3686C>G	XP_016860744.1:n.1450+3686C>G
XM_017005256.2:c.1336+3686C>G	XP_016860745.1:n.1336+3686C>G
XM_017005257.2:c.1387+3686C>G	XP_016860746.1:n.1387+3686C>G
XM_017005258.2:c.1336+3686C>G	XP_016860747.1:n.1336+3686C>G
XM_017005260.2:c.1162+3686C>G	XP_016860749.1:n.1162+3686C>G
XM_017005261.2:c.1099+3686C>G	XP_016860750.1:n.1099+3686C>G
XM_017005262.2:c.1099+3686C>G	XP_016860751.1:n.1099+3686C>G
XM_017005263.2:c.937+3686C>G	XP_016860752.1:n.937+3686C>G
XR_001739039.2:n.2880C>G
XR_001739040.1:n.3045C>G
XR_001739041.2:n.2841C>G
XR_001739042.2:n.2817C>G
XR_001739043.1:n.2793C>G
XR_001739044.2:n.2808C>G
XR_001739045.2:n.2778C>G
XR_001739046.1:n.3125C>G
XR_001739047.2:n.2694C>G
XR_001739048.1:n.2883C>G
XR_001739049.2:n.2628C>G
XR_001739050.2:n.2589C>G
XR_001739051.2:n.2556C>G
XR_001739052.2:n.2529C>G
XR_001739053.1:n.2518C>G
XR_001739054.1:n.2440C>G
XR_001739055.2:n.2457C>G
XR_001739056.2:n.2442C>G
XR_001739057.1:n.2458C>G
XR_001739058.1:n.2637C>G
XR_001739059.2:n.2370C>G
XR_001739060.1:n.2344C>G
XR_001739061.1:n.2386C>G
XR_001739062.1:n.2563C>G
XR_001739063.1:n.2270C>G
XR_001739064.1:n.2531C>G
XR_001739065.1:n.2475C>G
XR_001739066.1:n.2272C>G
XR_001739067.1:n.2179C>G
XR_001739068.1:n.2200C>G
XR_001739069.1:n.2377C>G
XR_001739070.1:n.2241C>G
XR_001739071.1:n.2099C>G
XR_001739072.1:n.2345C>G
XR_001739073.2:n.1591+3686C>G
XR_002959364.1:n.2271C>G
NM_001137550.2:c.1459+3686C>G MANE Select	NP_001131022.1:n.1459+3686C>G
NM_001137552.2:c.2178C>G	NP_001131024.1:p.Cys726Trp
NM_001137553.2:c.2010C>G	NP_001131025.1:p.Cys670Trp
NM_004735.4:c.2106C>G	NP_004726.2:p.Cys702Trp
NM_001137551.2:c.721+3686C>G	NP_001131023.1:n.721+3686C>G