Canonical Allele Identifier: CA374932450

Gene: LRSAM1

Linked Data

• MyVariant Identifiers: chr9:g.130248082G>C (hg19) ; chr9:g.127485803G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127485803G>C , CM000671.2:g.127485803G>C	GRCh38
NC_000009.11:g.130248082G>C , CM000671.1:g.130248082G>C	GRCh37
NC_000009.10:g.129287903G>C	NCBI36
NG_032008.1:g.39318G>C , LRG_373:g.39318G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000300417.11:c.1227G>C MANE Select	ENSP00000300417.6:p.Gln409His
ENST00000472068.2:c.*950G>C	ENSP00000501555.1:n.*950G>C
ENST00000498513.6:c.480G>C	ENSP00000501637.1:p.Gln160His
ENST00000674511.1:n.1102G>C
ENST00000674516.1:c.1227G>C	ENSP00000502441.1:p.Gln409His
ENST00000674621.1:n.1133G>C
ENST00000674771.1:c.1227G>C	ENSP00000502627.1:p.Gln409His
ENST00000674784.1:c.*386G>C	ENSP00000501837.1:n.*386G>C
ENST00000674970.1:c.*1001G>C	ENSP00000502493.1:n.*1001G>C
ENST00000675012.1:n.1107G>C
ENST00000675141.1:c.1227G>C	ENSP00000502420.1:p.Gln409His
ENST00000675198.1:n.1129G>C
ENST00000675213.1:c.1182G>C	ENSP00000502218.1:p.Gln394His
ENST00000675224.1:c.1227G>C	ENSP00000501869.1:p.Gln409His
ENST00000675253.1:c.1227G>C	ENSP00000502557.1:p.Gln409His
ENST00000675445.1:c.*899G>C	ENSP00000502253.1:n.*899G>C
ENST00000675448.1:c.1227G>C	ENSP00000502167.1:p.Gln409His
ENST00000675521.1:n.1079G>C
ENST00000675572.1:c.1227G>C	ENSP00000501598.1:p.Gln409His
ENST00000675641.1:c.1227G>C	ENSP00000501845.1:p.Gln409His
ENST00000675657.1:c.1227G>C	ENSP00000502002.1:p.Gln409His
ENST00000675662.1:n.1082+38G>C
ENST00000675789.1:c.1227G>C	ENSP00000501954.1:p.Gln409His
ENST00000675883.1:c.1227G>C	ENSP00000501592.1:p.Gln409His
ENST00000675945.1:c.1227G>C	ENSP00000501835.1:p.Gln409His
ENST00000676014.1:c.1170G>C	ENSP00000502058.1:p.Gln390His
ENST00000676035.1:n.988G>C
ENST00000676106.1:n.1032G>C
ENST00000676137.1:n.1118G>C
ENST00000676170.1:c.1308G>C	ENSP00000502177.1:p.Gln436His
ENST00000676318.1:c.1227G>C	ENSP00000502300.1:p.Gln409His
ENST00000676336.1:c.1005G>C	ENSP00000502686.1:p.Gln335His
ENST00000676349.1:c.*996G>C	ENSP00000502155.1:n.*996G>C
ENST00000676399.1:n.1125G>C
ENST00000676409.1:n.1106G>C
ENST00000300417.10:c.1227G>C	ENSP00000300417.6:p.Gln409His
ENST00000323301.8:c.1227G>C	ENSP00000322937.4:p.Gln409His
ENST00000373322.1:c.1227G>C	ENSP00000362419.1:p.Gln409His
ENST00000373324.8:c.1227G>C	ENSP00000362421.4:p.Gln409His
ENST00000472068.1:n.214G>C
ENST00000483302.5:n.444G>C
ENST00000498513.5:n.480G>C
NM_001005373.3:c.1227G>C	NP_001005373.1:p.Gln409His
NM_001005374.3:c.1227G>C	NP_001005374.1:p.Gln409His
NM_001190723.2:c.1227G>C	NP_001177652.1:p.Gln409His
NM_138361.5:c.1227G>C , LRG_373t1:c.1227G>C	NP_612370.3:p.Gln409His
XM_006717316.2:c.1227G>C	XP_006717379.1:p.Gln409His
XR_929874.1:n.1599G>C
XM_006717316.4:c.1227G>C	XP_006717379.1:p.Gln409His
XM_017015283.1:c.1227G>C	XP_016870772.1:p.Gln409His
XM_017015284.2:c.438G>C	XP_016870773.1:p.Gln146His
XR_001746415.2:n.1581G>C
XR_929874.3:n.1581G>C
NM_001190723.3:c.1227G>C	NP_001177652.1:p.Gln409His
NM_001005373.4:c.1227G>C MANE Select	NP_001005373.1:p.Gln409His
NM_001005374.4:c.1227G>C	NP_001005374.1:p.Gln409His
NM_001384142.1:c.1227G>C	NP_001371071.1:p.Gln409His
NM_001384143.1:c.1227G>C	NP_001371072.1:p.Gln409His
NM_001384144.1:c.438G>C	NP_001371073.1:p.Gln146His
NR_168891.1:n.1575G>C
NR_168892.1:n.1575G>C