Canonical Allele Identifier: CA5246406

Gene: LRSAM1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127455582T>C , CM000671.2:g.127455582T>C	GRCh38
NC_000009.11:g.130217861T>C , CM000671.1:g.130217861T>C	GRCh37
NC_000009.10:g.129257682T>C	NCBI36
NG_032008.1:g.9097T>C , LRG_373:g.9097T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300417.11:c.136T>C MANE Select	ENSP00000300417.6:p.Phe46Leu
ENST00000472068.2:c.122T>C	ENSP00000501555.1:p.Ile41Thr
ENST00000485704.2:n.570T>C
ENST00000498513.6:c.-612T>C	ENSP00000501637.1:n.-612T>C
ENST00000674516.1:c.136T>C	ENSP00000502441.1:p.Phe46Leu
ENST00000674771.1:c.136T>C	ENSP00000502627.1:p.Phe46Leu
ENST00000674784.1:c.136T>C	ENSP00000501837.1:p.Phe46Leu
ENST00000674970.1:c.136T>C	ENSP00000502493.1:p.Phe46Leu
ENST00000675141.1:c.136T>C	ENSP00000502420.1:p.Phe46Leu
ENST00000675213.1:c.129+528T>C	ENSP00000502218.1:n.129+528T>C
ENST00000675224.1:c.136T>C	ENSP00000501869.1:p.Phe46Leu
ENST00000675253.1:c.136T>C	ENSP00000502557.1:p.Phe46Leu
ENST00000675445.1:c.136T>C	ENSP00000502253.1:p.Phe46Leu
ENST00000675448.1:c.136T>C	ENSP00000502167.1:p.Phe46Leu
ENST00000675558.1:n.310T>C
ENST00000675572.1:c.136T>C	ENSP00000501598.1:p.Phe46Leu
ENST00000675641.1:c.136T>C	ENSP00000501845.1:p.Phe46Leu
ENST00000675657.1:c.136T>C	ENSP00000502002.1:p.Phe46Leu
ENST00000675789.1:c.136T>C	ENSP00000501954.1:p.Phe46Leu
ENST00000675883.1:c.136T>C	ENSP00000501592.1:p.Phe46Leu
ENST00000675945.1:c.136T>C	ENSP00000501835.1:p.Phe46Leu
ENST00000676014.1:c.79T>C	ENSP00000502058.1:p.Phe27Leu
ENST00000676170.1:c.136T>C	ENSP00000502177.1:p.Phe46Leu
ENST00000676318.1:c.136T>C	ENSP00000502300.1:p.Phe46Leu
ENST00000676336.1:c.136T>C	ENSP00000502686.1:p.Phe46Leu
ENST00000676349.1:c.136T>C	ENSP00000502155.1:p.Phe46Leu
ENST00000300417.10:c.136T>C	ENSP00000300417.6:p.Phe46Leu
ENST00000323301.8:c.136T>C	ENSP00000322937.4:p.Phe46Leu
ENST00000373322.1:c.136T>C	ENSP00000362419.1:p.Phe46Leu
ENST00000373324.8:c.136T>C	ENSP00000362421.4:p.Phe46Leu
ENST00000485704.1:n.315+528T>C
NM_001005373.3:c.136T>C	NP_001005373.1:p.Phe46Leu
NM_001005374.3:c.136T>C	NP_001005374.1:p.Phe46Leu
NM_001190723.2:c.136T>C	NP_001177652.1:p.Phe46Leu
NM_138361.5:c.136T>C , LRG_373t1:c.136T>C	NP_612370.3:p.Phe46Leu
XM_006717316.2:c.136T>C	XP_006717379.1:p.Phe46Leu
XR_929874.1:n.508T>C
XM_006717316.4:c.136T>C	XP_006717379.1:p.Phe46Leu
XM_017015283.1:c.136T>C	XP_016870772.1:p.Phe46Leu
XM_017015284.2:c.-649T>C	XP_016870773.1:n.-649T>C
XR_001746415.2:n.490T>C
XR_929874.3:n.490T>C
NM_001190723.3:c.136T>C	NP_001177652.1:p.Phe46Leu
NM_001005373.4:c.136T>C MANE Select	NP_001005373.1:p.Phe46Leu
NM_001005374.4:c.136T>C	NP_001005374.1:p.Phe46Leu
NM_001384142.1:c.136T>C	NP_001371071.1:p.Phe46Leu
NM_001384143.1:c.136T>C	NP_001371072.1:p.Phe46Leu
NM_001384144.1:c.-649T>C	NP_001371073.1:n.-649T>C
NR_168891.1:n.484T>C
NR_168892.1:n.484T>C