Canonical Allele Identifier: CA374932504

Gene: LRSAM1

Linked Data

• MyVariant Identifiers: chr9:g.130248092T>A (hg19) ; chr9:g.127485813T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127485813T>A , CM000671.2:g.127485813T>A	GRCh38
NC_000009.11:g.130248092T>A , CM000671.1:g.130248092T>A	GRCh37
NC_000009.10:g.129287913T>A	NCBI36
NG_032008.1:g.39328T>A , LRG_373:g.39328T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000300417.11:c.1237T>A MANE Select	ENSP00000300417.6:p.Leu413Met
ENST00000472068.2:c.*960T>A	ENSP00000501555.1:n.*960T>A
ENST00000498513.6:c.490T>A	ENSP00000501637.1:p.Leu164Met
ENST00000674511.1:n.1112T>A
ENST00000674516.1:c.1237T>A	ENSP00000502441.1:p.Leu413Met
ENST00000674621.1:n.1143T>A
ENST00000674771.1:c.1237T>A	ENSP00000502627.1:p.Leu413Met
ENST00000674784.1:c.*396T>A	ENSP00000501837.1:n.*396T>A
ENST00000674970.1:c.*1011T>A	ENSP00000502493.1:n.*1011T>A
ENST00000675012.1:n.1117T>A
ENST00000675141.1:c.1237T>A	ENSP00000502420.1:p.Leu413Met
ENST00000675198.1:n.1139T>A
ENST00000675213.1:c.1192T>A	ENSP00000502218.1:p.Leu398Met
ENST00000675224.1:c.1237T>A	ENSP00000501869.1:p.Leu413Met
ENST00000675253.1:c.1237T>A	ENSP00000502557.1:p.Leu413Met
ENST00000675445.1:c.*909T>A	ENSP00000502253.1:n.*909T>A
ENST00000675448.1:c.1237T>A	ENSP00000502167.1:p.Leu413Met
ENST00000675521.1:n.1089T>A
ENST00000675572.1:c.1237T>A	ENSP00000501598.1:p.Leu413Met
ENST00000675641.1:c.1237T>A	ENSP00000501845.1:p.Leu413Met
ENST00000675657.1:c.1237T>A	ENSP00000502002.1:p.Leu413Met
ENST00000675662.1:n.1082+48T>A
ENST00000675789.1:c.1237T>A	ENSP00000501954.1:p.Leu413Met
ENST00000675883.1:c.1237T>A	ENSP00000501592.1:p.Leu413Met
ENST00000675945.1:c.1237T>A	ENSP00000501835.1:p.Leu413Met
ENST00000676014.1:c.1180T>A	ENSP00000502058.1:p.Leu394Met
ENST00000676035.1:n.998T>A
ENST00000676106.1:n.1042T>A
ENST00000676137.1:n.1128T>A
ENST00000676170.1:c.1318T>A	ENSP00000502177.1:p.Leu440Met
ENST00000676318.1:c.1237T>A	ENSP00000502300.1:p.Leu413Met
ENST00000676336.1:c.1015T>A	ENSP00000502686.1:p.Leu339Met
ENST00000676349.1:c.*1006T>A	ENSP00000502155.1:n.*1006T>A
ENST00000676399.1:n.1135T>A
ENST00000676409.1:n.1116T>A
ENST00000300417.10:c.1237T>A	ENSP00000300417.6:p.Leu413Met
ENST00000323301.8:c.1237T>A	ENSP00000322937.4:p.Leu413Met
ENST00000373322.1:c.1237T>A	ENSP00000362419.1:p.Leu413Met
ENST00000373324.8:c.1237T>A	ENSP00000362421.4:p.Leu413Met
ENST00000472068.1:n.224T>A
ENST00000483302.5:n.454T>A
ENST00000498513.5:n.490T>A
NM_001005373.3:c.1237T>A	NP_001005373.1:p.Leu413Met
NM_001005374.3:c.1237T>A	NP_001005374.1:p.Leu413Met
NM_001190723.2:c.1237T>A	NP_001177652.1:p.Leu413Met
NM_138361.5:c.1237T>A , LRG_373t1:c.1237T>A	NP_612370.3:p.Leu413Met
XM_006717316.2:c.1237T>A	XP_006717379.1:p.Leu413Met
XR_929874.1:n.1609T>A
XM_006717316.4:c.1237T>A	XP_006717379.1:p.Leu413Met
XM_017015283.1:c.1237T>A	XP_016870772.1:p.Leu413Met
XM_017015284.2:c.448T>A	XP_016870773.1:p.Leu150Met
XR_001746415.2:n.1591T>A
XR_929874.3:n.1591T>A
NM_001190723.3:c.1237T>A	NP_001177652.1:p.Leu413Met
NM_001005373.4:c.1237T>A MANE Select	NP_001005373.1:p.Leu413Met
NM_001005374.4:c.1237T>A	NP_001005374.1:p.Leu413Met
NM_001384142.1:c.1237T>A	NP_001371071.1:p.Leu413Met
NM_001384143.1:c.1237T>A	NP_001371072.1:p.Leu413Met
NM_001384144.1:c.448T>A	NP_001371073.1:p.Leu150Met
NR_168891.1:n.1585T>A
NR_168892.1:n.1585T>A