Canonical Allele Identifier: CA467236628

Gene: LRSAM1

Linked Data

• MyVariant Identifiers: chr9:g.130263314C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127501035C>A , CM000671.2:g.127501035C>A	GRCh38
NC_000009.11:g.130263314C>A , CM000671.1:g.130263314C>A	GRCh37
NC_000009.10:g.129303135C>A	NCBI36
NG_032008.1:g.54550C>A , LRG_373:g.54550C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300417.11:c.1938C>A MANE Select	ENSP00000300417.6:p.Val646=
ENST00000472068.2:c.*1662C>A	ENSP00000501555.1:n.*1662C>A
ENST00000483302.6:n.2603C>A
ENST00000498513.6:c.*829C>A	ENSP00000501637.1:n.*829C>A
ENST00000674511.1:n.1537C>A
ENST00000674516.1:c.*554C>A	ENSP00000502441.1:n.*554C>A
ENST00000674621.1:n.1861-2338C>A
ENST00000674771.1:c.*581C>A	ENSP00000502627.1:n.*581C>A
ENST00000674784.1:c.*998C>A	ENSP00000501837.1:n.*998C>A
ENST00000674970.1:c.*1712C>A	ENSP00000502493.1:n.*1712C>A
ENST00000675012.1:n.1882C>A
ENST00000675141.1:c.1839C>A	ENSP00000502420.1:p.Val613=
ENST00000675198.1:n.1818C>A
ENST00000675213.1:c.1893C>A	ENSP00000502218.1:p.Val631=
ENST00000675224.1:c.*4C>A	ENSP00000501869.1:n.*4C>A
ENST00000675253.1:c.*610C>A	ENSP00000502557.1:n.*610C>A
ENST00000675445.1:c.*1610C>A	ENSP00000502253.1:n.*1610C>A
ENST00000675448.1:c.1938C>A	ENSP00000502167.1:p.Val646=
ENST00000675521.1:n.1848C>A
ENST00000675572.1:c.1839C>A	ENSP00000501598.1:p.Val613=
ENST00000675641.1:c.*680C>A	ENSP00000501845.1:n.*680C>A
ENST00000675657.1:c.*551C>A	ENSP00000502002.1:n.*551C>A
ENST00000675662.1:n.1733C>A
ENST00000675789.1:c.1758C>A	ENSP00000501954.1:p.Val586=
ENST00000675883.1:c.1857C>A	ENSP00000501592.1:p.Val619=
ENST00000675945.1:c.*579C>A	ENSP00000501835.1:n.*579C>A
ENST00000676014.1:c.1881C>A	ENSP00000502058.1:p.Val627=
ENST00000676035.1:n.1600C>A
ENST00000676106.1:n.1975C>A
ENST00000676137.1:n.1968C>A
ENST00000676170.1:c.2019C>A	ENSP00000502177.1:p.Val673=
ENST00000676318.1:c.*2768C>A	ENSP00000502300.1:n.*2768C>A
ENST00000676336.1:c.*551C>A	ENSP00000502686.1:n.*551C>A
ENST00000676349.1:c.*1626C>A	ENSP00000502155.1:n.*1626C>A
ENST00000676399.1:n.1841C>A
ENST00000676409.1:n.1998C>A
ENST00000300417.10:c.1938C>A	ENSP00000300417.6:p.Val646=
ENST00000323301.8:c.1938C>A	ENSP00000322937.4:p.Val646=
ENST00000373322.1:c.1938C>A	ENSP00000362419.1:p.Val646=
ENST00000373324.8:c.1857C>A	ENSP00000362421.4:p.Val619=
ENST00000472068.1:n.831C>A
ENST00000483302.5:n.1160C>A
NM_001005373.3:c.1938C>A	NP_001005373.1:p.Val646=
NM_001005374.3:c.1938C>A	NP_001005374.1:p.Val646=
NM_001190723.2:c.1857C>A	NP_001177652.1:p.Val619=
NM_138361.5:c.1938C>A , LRG_373t1:c.1938C>A	NP_612370.3:p.Val646=
XM_006717316.2:c.1839C>A	XP_006717379.1:p.Val613=
XM_006717316.4:c.1839C>A	XP_006717379.1:p.Val613=
XM_017015283.1:c.1938C>A	XP_016870772.1:p.Val646=
XM_017015284.2:c.1149C>A	XP_016870773.1:p.Val383=
XR_001746415.2:n.2473C>A
XR_929874.3:n.2297C>A
NM_001190723.3:c.1857C>A	NP_001177652.1:p.Val619=
NM_001005373.4:c.1938C>A MANE Select	NP_001005373.1:p.Val646=
NM_001005374.4:c.1938C>A	NP_001005374.1:p.Val646=
NM_001384142.1:c.1938C>A	NP_001371071.1:p.Val646=
NM_001384143.1:c.1839C>A	NP_001371072.1:p.Val613=
NM_001384144.1:c.1149C>A	NP_001371073.1:p.Val383=
NR_168891.1:n.2467C>A
NR_168892.1:n.2291C>A