Canonical Allele Identifier: CA374938195

Gene: LRSAM1

Linked Data

• MyVariant Identifiers: chr9:g.130263331C>A (hg19) ; chr9:g.127501052C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127501052C>A , CM000671.2:g.127501052C>A	GRCh38
NC_000009.11:g.130263331C>A , CM000671.1:g.130263331C>A	GRCh37
NC_000009.10:g.129303152C>A	NCBI36
NG_032008.1:g.54567C>A , LRG_373:g.54567C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300417.11:c.1955C>A MANE Select	ENSP00000300417.6:p.Pro652His
ENST00000472068.2:c.*1679C>A	ENSP00000501555.1:n.*1679C>A
ENST00000483302.6:n.2620C>A
ENST00000498513.6:c.*846C>A	ENSP00000501637.1:n.*846C>A
ENST00000674511.1:n.1554C>A
ENST00000674516.1:c.*571C>A	ENSP00000502441.1:n.*571C>A
ENST00000674621.1:n.1861-2321C>A
ENST00000674771.1:c.*598C>A	ENSP00000502627.1:n.*598C>A
ENST00000674784.1:c.*1015C>A	ENSP00000501837.1:n.*1015C>A
ENST00000674970.1:c.*1729C>A	ENSP00000502493.1:n.*1729C>A
ENST00000675012.1:n.1899C>A
ENST00000675141.1:c.1856C>A	ENSP00000502420.1:p.Pro619His
ENST00000675198.1:n.1835C>A
ENST00000675213.1:c.1910C>A	ENSP00000502218.1:p.Pro637His
ENST00000675224.1:c.*21C>A	ENSP00000501869.1:n.*21C>A
ENST00000675253.1:c.*627C>A	ENSP00000502557.1:n.*627C>A
ENST00000675445.1:c.*1627C>A	ENSP00000502253.1:n.*1627C>A
ENST00000675448.1:c.1955C>A	ENSP00000502167.1:p.Pro652His
ENST00000675521.1:n.1865C>A
ENST00000675572.1:c.1856C>A	ENSP00000501598.1:p.Pro619His
ENST00000675641.1:c.*697C>A	ENSP00000501845.1:n.*697C>A
ENST00000675657.1:c.*568C>A	ENSP00000502002.1:n.*568C>A
ENST00000675662.1:n.1750C>A
ENST00000675789.1:c.1775C>A	ENSP00000501954.1:p.Pro592His
ENST00000675883.1:c.1874C>A	ENSP00000501592.1:p.Pro625His
ENST00000675945.1:c.*596C>A	ENSP00000501835.1:n.*596C>A
ENST00000676014.1:c.1898C>A	ENSP00000502058.1:p.Pro633His
ENST00000676035.1:n.1617C>A
ENST00000676106.1:n.1992C>A
ENST00000676137.1:n.1985C>A
ENST00000676170.1:c.2036C>A	ENSP00000502177.1:p.Pro679His
ENST00000676318.1:c.*2785C>A	ENSP00000502300.1:n.*2785C>A
ENST00000676336.1:c.*568C>A	ENSP00000502686.1:n.*568C>A
ENST00000676349.1:c.*1643C>A	ENSP00000502155.1:n.*1643C>A
ENST00000676399.1:n.1858C>A
ENST00000676409.1:n.2015C>A
ENST00000300417.10:c.1955C>A	ENSP00000300417.6:p.Pro652His
ENST00000323301.8:c.1955C>A	ENSP00000322937.4:p.Pro652His
ENST00000373322.1:c.1955C>A	ENSP00000362419.1:p.Pro652His
ENST00000373324.8:c.1874C>A	ENSP00000362421.4:p.Pro625His
ENST00000472068.1:n.848C>A
ENST00000483302.5:n.1177C>A
NM_001005373.3:c.1955C>A	NP_001005373.1:p.Pro652His
NM_001005374.3:c.1955C>A	NP_001005374.1:p.Pro652His
NM_001190723.2:c.1874C>A	NP_001177652.1:p.Pro625His
NM_138361.5:c.1955C>A , LRG_373t1:c.1955C>A	NP_612370.3:p.Pro652His
XM_006717316.2:c.1856C>A	XP_006717379.1:p.Pro619His
XM_006717316.4:c.1856C>A	XP_006717379.1:p.Pro619His
XM_017015283.1:c.1955C>A	XP_016870772.1:p.Pro652His
XM_017015284.2:c.1166C>A	XP_016870773.1:p.Pro389His
XR_001746415.2:n.2490C>A
XR_929874.3:n.2314C>A
NM_001190723.3:c.1874C>A	NP_001177652.1:p.Pro625His
NM_001005373.4:c.1955C>A MANE Select	NP_001005373.1:p.Pro652His
NM_001005374.4:c.1955C>A	NP_001005374.1:p.Pro652His
NM_001384142.1:c.1955C>A	NP_001371071.1:p.Pro652His
NM_001384143.1:c.1856C>A	NP_001371072.1:p.Pro619His
NM_001384144.1:c.1166C>A	NP_001371073.1:p.Pro389His
NR_168891.1:n.2484C>A
NR_168892.1:n.2308C>A