Canonical Allele Identifier: CA467236699

Gene: LRSAM1

Linked Data

• MyVariant Identifiers: chr9:g.130263332C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127501053C>A , CM000671.2:g.127501053C>A	GRCh38
NC_000009.11:g.130263332C>A , CM000671.1:g.130263332C>A	GRCh37
NC_000009.10:g.129303153C>A	NCBI36
NG_032008.1:g.54568C>A , LRG_373:g.54568C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300417.11:c.1956C>A MANE Select	ENSP00000300417.6:p.Pro652=
ENST00000472068.2:c.*1680C>A	ENSP00000501555.1:n.*1680C>A
ENST00000483302.6:n.2621C>A
ENST00000498513.6:c.*847C>A	ENSP00000501637.1:n.*847C>A
ENST00000674511.1:n.1555C>A
ENST00000674516.1:c.*572C>A	ENSP00000502441.1:n.*572C>A
ENST00000674621.1:n.1861-2320C>A
ENST00000674771.1:c.*599C>A	ENSP00000502627.1:n.*599C>A
ENST00000674784.1:c.*1016C>A	ENSP00000501837.1:n.*1016C>A
ENST00000674970.1:c.*1730C>A	ENSP00000502493.1:n.*1730C>A
ENST00000675012.1:n.1900C>A
ENST00000675141.1:c.1857C>A	ENSP00000502420.1:p.Pro619=
ENST00000675198.1:n.1836C>A
ENST00000675213.1:c.1911C>A	ENSP00000502218.1:p.Pro637=
ENST00000675224.1:c.*22C>A	ENSP00000501869.1:n.*22C>A
ENST00000675253.1:c.*628C>A	ENSP00000502557.1:n.*628C>A
ENST00000675445.1:c.*1628C>A	ENSP00000502253.1:n.*1628C>A
ENST00000675448.1:c.1956C>A	ENSP00000502167.1:p.Pro652=
ENST00000675521.1:n.1866C>A
ENST00000675572.1:c.1857C>A	ENSP00000501598.1:p.Pro619=
ENST00000675641.1:c.*698C>A	ENSP00000501845.1:n.*698C>A
ENST00000675657.1:c.*569C>A	ENSP00000502002.1:n.*569C>A
ENST00000675662.1:n.1751C>A
ENST00000675789.1:c.1776C>A	ENSP00000501954.1:p.Pro592=
ENST00000675883.1:c.1875C>A	ENSP00000501592.1:p.Pro625=
ENST00000675945.1:c.*597C>A	ENSP00000501835.1:n.*597C>A
ENST00000676014.1:c.1899C>A	ENSP00000502058.1:p.Pro633=
ENST00000676035.1:n.1618C>A
ENST00000676106.1:n.1993C>A
ENST00000676137.1:n.1986C>A
ENST00000676170.1:c.2037C>A	ENSP00000502177.1:p.Pro679=
ENST00000676318.1:c.*2786C>A	ENSP00000502300.1:n.*2786C>A
ENST00000676336.1:c.*569C>A	ENSP00000502686.1:n.*569C>A
ENST00000676349.1:c.*1644C>A	ENSP00000502155.1:n.*1644C>A
ENST00000676399.1:n.1859C>A
ENST00000676409.1:n.2016C>A
ENST00000300417.10:c.1956C>A	ENSP00000300417.6:p.Pro652=
ENST00000323301.8:c.1956C>A	ENSP00000322937.4:p.Pro652=
ENST00000373322.1:c.1956C>A	ENSP00000362419.1:p.Pro652=
ENST00000373324.8:c.1875C>A	ENSP00000362421.4:p.Pro625=
ENST00000472068.1:n.849C>A
ENST00000483302.5:n.1178C>A
NM_001005373.3:c.1956C>A	NP_001005373.1:p.Pro652=
NM_001005374.3:c.1956C>A	NP_001005374.1:p.Pro652=
NM_001190723.2:c.1875C>A	NP_001177652.1:p.Pro625=
NM_138361.5:c.1956C>A , LRG_373t1:c.1956C>A	NP_612370.3:p.Pro652=
XM_006717316.2:c.1857C>A	XP_006717379.1:p.Pro619=
XM_006717316.4:c.1857C>A	XP_006717379.1:p.Pro619=
XM_017015283.1:c.1956C>A	XP_016870772.1:p.Pro652=
XM_017015284.2:c.1167C>A	XP_016870773.1:p.Pro389=
XR_001746415.2:n.2491C>A
XR_929874.3:n.2315C>A
NM_001190723.3:c.1875C>A	NP_001177652.1:p.Pro625=
NM_001005373.4:c.1956C>A MANE Select	NP_001005373.1:p.Pro652=
NM_001005374.4:c.1956C>A	NP_001005374.1:p.Pro652=
NM_001384142.1:c.1956C>A	NP_001371071.1:p.Pro652=
NM_001384143.1:c.1857C>A	NP_001371072.1:p.Pro619=
NM_001384144.1:c.1167C>A	NP_001371073.1:p.Pro389=
NR_168891.1:n.2485C>A
NR_168892.1:n.2309C>A