Canonical Allele Identifier: CA374938288

Gene: LRSAM1

Linked Data

• MyVariant Identifiers: chr9:g.130263379T>C (hg19) ; chr9:g.127501100T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127501100T>C , CM000671.2:g.127501100T>C	GRCh38
NC_000009.11:g.130263379T>C , CM000671.1:g.130263379T>C	GRCh37
NC_000009.10:g.129303200T>C	NCBI36
NG_032008.1:g.54615T>C , LRG_373:g.54615T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300417.11:c.2003T>C MANE Select	ENSP00000300417.6:p.Leu668Pro
ENST00000472068.2:c.*1727T>C	ENSP00000501555.1:n.*1727T>C
ENST00000483302.6:n.2668T>C
ENST00000498513.6:c.*894T>C	ENSP00000501637.1:n.*894T>C
ENST00000674511.1:n.1602T>C
ENST00000674516.1:c.*619T>C	ENSP00000502441.1:n.*619T>C
ENST00000674621.1:n.1861-2273T>C
ENST00000674771.1:c.*646T>C	ENSP00000502627.1:n.*646T>C
ENST00000674784.1:c.*1063T>C	ENSP00000501837.1:n.*1063T>C
ENST00000674970.1:c.*1777T>C	ENSP00000502493.1:n.*1777T>C
ENST00000675012.1:n.1947T>C
ENST00000675141.1:c.1904T>C	ENSP00000502420.1:p.Leu635Pro
ENST00000675198.1:n.1883T>C
ENST00000675213.1:c.1958T>C	ENSP00000502218.1:p.Leu653Pro
ENST00000675224.1:c.*69T>C	ENSP00000501869.1:n.*69T>C
ENST00000675253.1:c.*675T>C	ENSP00000502557.1:n.*675T>C
ENST00000675445.1:c.*1675T>C	ENSP00000502253.1:n.*1675T>C
ENST00000675448.1:c.2003T>C	ENSP00000502167.1:p.Leu668Pro
ENST00000675521.1:n.1913T>C
ENST00000675572.1:c.1904T>C	ENSP00000501598.1:p.Leu635Pro
ENST00000675641.1:c.*745T>C	ENSP00000501845.1:n.*745T>C
ENST00000675657.1:c.*616T>C	ENSP00000502002.1:n.*616T>C
ENST00000675662.1:n.1798T>C
ENST00000675789.1:c.1823T>C	ENSP00000501954.1:p.Leu608Pro
ENST00000675883.1:c.1922T>C	ENSP00000501592.1:p.Leu641Pro
ENST00000675945.1:c.*644T>C	ENSP00000501835.1:n.*644T>C
ENST00000676014.1:c.1946T>C	ENSP00000502058.1:p.Leu649Pro
ENST00000676035.1:n.1665T>C
ENST00000676106.1:n.2040T>C
ENST00000676137.1:n.2033T>C
ENST00000676170.1:c.2084T>C	ENSP00000502177.1:p.Leu695Pro
ENST00000676318.1:c.*2833T>C	ENSP00000502300.1:n.*2833T>C
ENST00000676336.1:c.*616T>C	ENSP00000502686.1:n.*616T>C
ENST00000676349.1:c.*1691T>C	ENSP00000502155.1:n.*1691T>C
ENST00000676399.1:n.1906T>C
ENST00000676409.1:n.2063T>C
ENST00000300417.10:c.2003T>C	ENSP00000300417.6:p.Leu668Pro
ENST00000323301.8:c.2003T>C	ENSP00000322937.4:p.Leu668Pro
ENST00000373322.1:c.2003T>C	ENSP00000362419.1:p.Leu668Pro
ENST00000373324.8:c.1922T>C	ENSP00000362421.4:p.Leu641Pro
ENST00000483302.5:n.1225T>C
NM_001005373.3:c.2003T>C	NP_001005373.1:p.Leu668Pro
NM_001005374.3:c.2003T>C	NP_001005374.1:p.Leu668Pro
NM_001190723.2:c.1922T>C	NP_001177652.1:p.Leu641Pro
NM_138361.5:c.2003T>C , LRG_373t1:c.2003T>C	NP_612370.3:p.Leu668Pro
XM_006717316.2:c.1904T>C	XP_006717379.1:p.Leu635Pro
XM_006717316.4:c.1904T>C	XP_006717379.1:p.Leu635Pro
XM_017015283.1:c.2003T>C	XP_016870772.1:p.Leu668Pro
XM_017015284.2:c.1214T>C	XP_016870773.1:p.Leu405Pro
XR_001746415.2:n.2538T>C
XR_929874.3:n.2362T>C
NM_001190723.3:c.1922T>C	NP_001177652.1:p.Leu641Pro
NM_001005373.4:c.2003T>C MANE Select	NP_001005373.1:p.Leu668Pro
NM_001005374.4:c.2003T>C	NP_001005374.1:p.Leu668Pro
NM_001384142.1:c.2003T>C	NP_001371071.1:p.Leu668Pro
NM_001384143.1:c.1904T>C	NP_001371072.1:p.Leu635Pro
NM_001384144.1:c.1214T>C	NP_001371073.1:p.Leu405Pro
NR_168891.1:n.2532T>C
NR_168892.1:n.2356T>C