Canonical Allele Identifier: CA374938196

Gene: LRSAM1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300417.11:c.1955C>T MANE Select	ENSP00000300417.6:p.Pro652Leu
ENST00000472068.2:c.*1679C>T	ENSP00000501555.1:n.*1679C>T
ENST00000483302.6:n.2620C>T
ENST00000498513.6:c.*846C>T	ENSP00000501637.1:n.*846C>T
ENST00000674511.1:n.1554C>T
ENST00000674516.1:c.*571C>T	ENSP00000502441.1:n.*571C>T
ENST00000674621.1:n.1861-2321C>T
ENST00000674771.1:c.*598C>T	ENSP00000502627.1:n.*598C>T
ENST00000674784.1:c.*1015C>T	ENSP00000501837.1:n.*1015C>T
ENST00000674970.1:c.*1729C>T	ENSP00000502493.1:n.*1729C>T
ENST00000675012.1:n.1899C>T
ENST00000675141.1:c.1856C>T	ENSP00000502420.1:p.Pro619Leu
ENST00000675198.1:n.1835C>T
ENST00000675213.1:c.1910C>T	ENSP00000502218.1:p.Pro637Leu
ENST00000675224.1:c.*21C>T	ENSP00000501869.1:n.*21C>T
ENST00000675253.1:c.*627C>T	ENSP00000502557.1:n.*627C>T
ENST00000675445.1:c.*1627C>T	ENSP00000502253.1:n.*1627C>T
ENST00000675448.1:c.1955C>T	ENSP00000502167.1:p.Pro652Leu
ENST00000675521.1:n.1865C>T
ENST00000675572.1:c.1856C>T	ENSP00000501598.1:p.Pro619Leu
ENST00000675641.1:c.*697C>T	ENSP00000501845.1:n.*697C>T
ENST00000675657.1:c.*568C>T	ENSP00000502002.1:n.*568C>T
ENST00000675662.1:n.1750C>T
ENST00000675789.1:c.1775C>T	ENSP00000501954.1:p.Pro592Leu
ENST00000675883.1:c.1874C>T	ENSP00000501592.1:p.Pro625Leu
ENST00000675945.1:c.*596C>T	ENSP00000501835.1:n.*596C>T
ENST00000676014.1:c.1898C>T	ENSP00000502058.1:p.Pro633Leu
ENST00000676035.1:n.1617C>T
ENST00000676106.1:n.1992C>T
ENST00000676137.1:n.1985C>T
ENST00000676170.1:c.2036C>T	ENSP00000502177.1:p.Pro679Leu
ENST00000676318.1:c.*2785C>T	ENSP00000502300.1:n.*2785C>T
ENST00000676336.1:c.*568C>T	ENSP00000502686.1:n.*568C>T
ENST00000676349.1:c.*1643C>T	ENSP00000502155.1:n.*1643C>T
ENST00000676399.1:n.1858C>T
ENST00000676409.1:n.2015C>T
ENST00000300417.10:c.1955C>T	ENSP00000300417.6:p.Pro652Leu
ENST00000323301.8:c.1955C>T	ENSP00000322937.4:p.Pro652Leu
ENST00000373322.1:c.1955C>T	ENSP00000362419.1:p.Pro652Leu
ENST00000373324.8:c.1874C>T	ENSP00000362421.4:p.Pro625Leu
ENST00000472068.1:n.848C>T
ENST00000483302.5:n.1177C>T
NM_001005373.3:c.1955C>T	NP_001005373.1:p.Pro652Leu
NM_001005374.3:c.1955C>T	NP_001005374.1:p.Pro652Leu
NM_001190723.2:c.1874C>T	NP_001177652.1:p.Pro625Leu
NM_138361.5:c.1955C>T , LRG_373t1:c.1955C>T	NP_612370.3:p.Pro652Leu
XM_006717316.2:c.1856C>T	XP_006717379.1:p.Pro619Leu
XM_006717316.4:c.1856C>T	XP_006717379.1:p.Pro619Leu
XM_017015283.1:c.1955C>T	XP_016870772.1:p.Pro652Leu
XM_017015284.2:c.1166C>T	XP_016870773.1:p.Pro389Leu
XR_001746415.2:n.2490C>T
XR_929874.3:n.2314C>T
NM_001190723.3:c.1874C>T	NP_001177652.1:p.Pro625Leu
NM_001005373.4:c.1955C>T MANE Select	NP_001005373.1:p.Pro652Leu
NM_001005374.4:c.1955C>T	NP_001005374.1:p.Pro652Leu
NM_001384142.1:c.1955C>T	NP_001371071.1:p.Pro652Leu
NM_001384143.1:c.1856C>T	NP_001371072.1:p.Pro619Leu
NM_001384144.1:c.1166C>T	NP_001371073.1:p.Pro389Leu
NR_168891.1:n.2484C>T
NR_168892.1:n.2308C>T