Canonical Allele Identifier: CA467231764

Gene: LRSAM1

Linked Data

• MyVariant Identifiers: chr9:g.130248094G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127485815G>A , CM000671.2:g.127485815G>A	GRCh38
NC_000009.11:g.130248094G>A , CM000671.1:g.130248094G>A	GRCh37
NC_000009.10:g.129287915G>A	NCBI36
NG_032008.1:g.39330G>A , LRG_373:g.39330G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000300417.11:c.1239G>A MANE Select	ENSP00000300417.6:p.Leu413=
ENST00000472068.2:c.*962G>A	ENSP00000501555.1:n.*962G>A
ENST00000498513.6:c.492G>A	ENSP00000501637.1:p.Leu164=
ENST00000674511.1:n.1114G>A
ENST00000674516.1:c.1239G>A	ENSP00000502441.1:p.Leu413=
ENST00000674621.1:n.1145G>A
ENST00000674771.1:c.1239G>A	ENSP00000502627.1:p.Leu413=
ENST00000674784.1:c.*398G>A	ENSP00000501837.1:n.*398G>A
ENST00000674970.1:c.*1013G>A	ENSP00000502493.1:n.*1013G>A
ENST00000675012.1:n.1119G>A
ENST00000675141.1:c.1239G>A	ENSP00000502420.1:p.Leu413=
ENST00000675198.1:n.1141G>A
ENST00000675213.1:c.1194G>A	ENSP00000502218.1:p.Leu398=
ENST00000675224.1:c.1239G>A	ENSP00000501869.1:p.Leu413=
ENST00000675253.1:c.1239G>A	ENSP00000502557.1:p.Leu413=
ENST00000675445.1:c.*911G>A	ENSP00000502253.1:n.*911G>A
ENST00000675448.1:c.1239G>A	ENSP00000502167.1:p.Leu413=
ENST00000675521.1:n.1091G>A
ENST00000675572.1:c.1239G>A	ENSP00000501598.1:p.Leu413=
ENST00000675641.1:c.1239G>A	ENSP00000501845.1:p.Leu413=
ENST00000675657.1:c.1239G>A	ENSP00000502002.1:p.Leu413=
ENST00000675662.1:n.1082+50G>A
ENST00000675789.1:c.1239G>A	ENSP00000501954.1:p.Leu413=
ENST00000675883.1:c.1239G>A	ENSP00000501592.1:p.Leu413=
ENST00000675945.1:c.1239G>A	ENSP00000501835.1:p.Leu413=
ENST00000676014.1:c.1182G>A	ENSP00000502058.1:p.Leu394=
ENST00000676035.1:n.1000G>A
ENST00000676106.1:n.1044G>A
ENST00000676137.1:n.1130G>A
ENST00000676170.1:c.1320G>A	ENSP00000502177.1:p.Leu440=
ENST00000676318.1:c.1239G>A	ENSP00000502300.1:p.Leu413=
ENST00000676336.1:c.1017G>A	ENSP00000502686.1:p.Leu339=
ENST00000676349.1:c.*1008G>A	ENSP00000502155.1:n.*1008G>A
ENST00000676399.1:n.1137G>A
ENST00000676409.1:n.1118G>A
ENST00000300417.10:c.1239G>A	ENSP00000300417.6:p.Leu413=
ENST00000323301.8:c.1239G>A	ENSP00000322937.4:p.Leu413=
ENST00000373322.1:c.1239G>A	ENSP00000362419.1:p.Leu413=
ENST00000373324.8:c.1239G>A	ENSP00000362421.4:p.Leu413=
ENST00000472068.1:n.226G>A
ENST00000483302.5:n.456G>A
ENST00000498513.5:n.492G>A
NM_001005373.3:c.1239G>A	NP_001005373.1:p.Leu413=
NM_001005374.3:c.1239G>A	NP_001005374.1:p.Leu413=
NM_001190723.2:c.1239G>A	NP_001177652.1:p.Leu413=
NM_138361.5:c.1239G>A , LRG_373t1:c.1239G>A	NP_612370.3:p.Leu413=
XM_006717316.2:c.1239G>A	XP_006717379.1:p.Leu413=
XR_929874.1:n.1611G>A
XM_006717316.4:c.1239G>A	XP_006717379.1:p.Leu413=
XM_017015283.1:c.1239G>A	XP_016870772.1:p.Leu413=
XM_017015284.2:c.450G>A	XP_016870773.1:p.Leu150=
XR_001746415.2:n.1593G>A
XR_929874.3:n.1593G>A
NM_001190723.3:c.1239G>A	NP_001177652.1:p.Leu413=
NM_001005373.4:c.1239G>A MANE Select	NP_001005373.1:p.Leu413=
NM_001005374.4:c.1239G>A	NP_001005374.1:p.Leu413=
NM_001384142.1:c.1239G>A	NP_001371071.1:p.Leu413=
NM_001384143.1:c.1239G>A	NP_001371072.1:p.Leu413=
NM_001384144.1:c.450G>A	NP_001371073.1:p.Leu150=
NR_168891.1:n.1587G>A
NR_168892.1:n.1587G>A