Canonical Allele Identifier: CA374938189

Gene: LRSAM1

Linked Data

• MyVariant Identifiers: chr9:g.130263327G>T (hg19) ; chr9:g.127501048G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127501048G>T , CM000671.2:g.127501048G>T	GRCh38
NC_000009.11:g.130263327G>T , CM000671.1:g.130263327G>T	GRCh37
NC_000009.10:g.129303148G>T	NCBI36
NG_032008.1:g.54563G>T , LRG_373:g.54563G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300417.11:c.1951G>T MANE Select	ENSP00000300417.6:p.Ala651Ser
ENST00000472068.2:c.*1675G>T	ENSP00000501555.1:n.*1675G>T
ENST00000483302.6:n.2616G>T
ENST00000498513.6:c.*842G>T	ENSP00000501637.1:n.*842G>T
ENST00000674511.1:n.1550G>T
ENST00000674516.1:c.*567G>T	ENSP00000502441.1:n.*567G>T
ENST00000674621.1:n.1861-2325G>T
ENST00000674771.1:c.*594G>T	ENSP00000502627.1:n.*594G>T
ENST00000674784.1:c.*1011G>T	ENSP00000501837.1:n.*1011G>T
ENST00000674970.1:c.*1725G>T	ENSP00000502493.1:n.*1725G>T
ENST00000675012.1:n.1895G>T
ENST00000675141.1:c.1852G>T	ENSP00000502420.1:p.Ala618Ser
ENST00000675198.1:n.1831G>T
ENST00000675213.1:c.1906G>T	ENSP00000502218.1:p.Ala636Ser
ENST00000675224.1:c.*17G>T	ENSP00000501869.1:n.*17G>T
ENST00000675253.1:c.*623G>T	ENSP00000502557.1:n.*623G>T
ENST00000675445.1:c.*1623G>T	ENSP00000502253.1:n.*1623G>T
ENST00000675448.1:c.1951G>T	ENSP00000502167.1:p.Ala651Ser
ENST00000675521.1:n.1861G>T
ENST00000675572.1:c.1852G>T	ENSP00000501598.1:p.Ala618Ser
ENST00000675641.1:c.*693G>T	ENSP00000501845.1:n.*693G>T
ENST00000675657.1:c.*564G>T	ENSP00000502002.1:n.*564G>T
ENST00000675662.1:n.1746G>T
ENST00000675789.1:c.1771G>T	ENSP00000501954.1:p.Ala591Ser
ENST00000675883.1:c.1870G>T	ENSP00000501592.1:p.Ala624Ser
ENST00000675945.1:c.*592G>T	ENSP00000501835.1:n.*592G>T
ENST00000676014.1:c.1894G>T	ENSP00000502058.1:p.Ala632Ser
ENST00000676035.1:n.1613G>T
ENST00000676106.1:n.1988G>T
ENST00000676137.1:n.1981G>T
ENST00000676170.1:c.2032G>T	ENSP00000502177.1:p.Ala678Ser
ENST00000676318.1:c.*2781G>T	ENSP00000502300.1:n.*2781G>T
ENST00000676336.1:c.*564G>T	ENSP00000502686.1:n.*564G>T
ENST00000676349.1:c.*1639G>T	ENSP00000502155.1:n.*1639G>T
ENST00000676399.1:n.1854G>T
ENST00000676409.1:n.2011G>T
ENST00000300417.10:c.1951G>T	ENSP00000300417.6:p.Ala651Ser
ENST00000323301.8:c.1951G>T	ENSP00000322937.4:p.Ala651Ser
ENST00000373322.1:c.1951G>T	ENSP00000362419.1:p.Ala651Ser
ENST00000373324.8:c.1870G>T	ENSP00000362421.4:p.Ala624Ser
ENST00000472068.1:n.844G>T
ENST00000483302.5:n.1173G>T
NM_001005373.3:c.1951G>T	NP_001005373.1:p.Ala651Ser
NM_001005374.3:c.1951G>T	NP_001005374.1:p.Ala651Ser
NM_001190723.2:c.1870G>T	NP_001177652.1:p.Ala624Ser
NM_138361.5:c.1951G>T , LRG_373t1:c.1951G>T	NP_612370.3:p.Ala651Ser
XM_006717316.2:c.1852G>T	XP_006717379.1:p.Ala618Ser
XM_006717316.4:c.1852G>T	XP_006717379.1:p.Ala618Ser
XM_017015283.1:c.1951G>T	XP_016870772.1:p.Ala651Ser
XM_017015284.2:c.1162G>T	XP_016870773.1:p.Ala388Ser
XR_001746415.2:n.2486G>T
XR_929874.3:n.2310G>T
NM_001190723.3:c.1870G>T	NP_001177652.1:p.Ala624Ser
NM_001005373.4:c.1951G>T MANE Select	NP_001005373.1:p.Ala651Ser
NM_001005374.4:c.1951G>T	NP_001005374.1:p.Ala651Ser
NM_001384142.1:c.1951G>T	NP_001371071.1:p.Ala651Ser
NM_001384143.1:c.1852G>T	NP_001371072.1:p.Ala618Ser
NM_001384144.1:c.1162G>T	NP_001371073.1:p.Ala388Ser
NR_168891.1:n.2480G>T
NR_168892.1:n.2304G>T