Canonical Allele Identifier: CA374938224

Gene: LRSAM1

Linked Data

• dbSNP Id: rs1193233488
• MyVariant Identifiers: chr9:g.130263345G>T (hg19) ; chr9:g.127501066G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127501066G>T , CM000671.2:g.127501066G>T	GRCh38
NC_000009.11:g.130263345G>T , CM000671.1:g.130263345G>T	GRCh37
NC_000009.10:g.129303166G>T	NCBI36
NG_032008.1:g.54581G>T , LRG_373:g.54581G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300417.11:c.1969G>T MANE Select	ENSP00000300417.6:p.Glu657Ter
ENST00000472068.2:c.*1693G>T	ENSP00000501555.1:n.*1693G>T
ENST00000483302.6:n.2634G>T
ENST00000498513.6:c.*860G>T	ENSP00000501637.1:n.*860G>T
ENST00000674511.1:n.1568G>T
ENST00000674516.1:c.*585G>T	ENSP00000502441.1:n.*585G>T
ENST00000674621.1:n.1861-2307G>T
ENST00000674771.1:c.*612G>T	ENSP00000502627.1:n.*612G>T
ENST00000674784.1:c.*1029G>T	ENSP00000501837.1:n.*1029G>T
ENST00000674970.1:c.*1743G>T	ENSP00000502493.1:n.*1743G>T
ENST00000675012.1:n.1913G>T
ENST00000675141.1:c.1870G>T	ENSP00000502420.1:p.Glu624Ter
ENST00000675198.1:n.1849G>T
ENST00000675213.1:c.1924G>T	ENSP00000502218.1:p.Glu642Ter
ENST00000675224.1:c.*35G>T	ENSP00000501869.1:n.*35G>T
ENST00000675253.1:c.*641G>T	ENSP00000502557.1:n.*641G>T
ENST00000675445.1:c.*1641G>T	ENSP00000502253.1:n.*1641G>T
ENST00000675448.1:c.1969G>T	ENSP00000502167.1:p.Glu657Ter
ENST00000675521.1:n.1879G>T
ENST00000675572.1:c.1870G>T	ENSP00000501598.1:p.Glu624Ter
ENST00000675641.1:c.*711G>T	ENSP00000501845.1:n.*711G>T
ENST00000675657.1:c.*582G>T	ENSP00000502002.1:n.*582G>T
ENST00000675662.1:n.1764G>T
ENST00000675789.1:c.1789G>T	ENSP00000501954.1:p.Glu597Ter
ENST00000675883.1:c.1888G>T	ENSP00000501592.1:p.Glu630Ter
ENST00000675945.1:c.*610G>T	ENSP00000501835.1:n.*610G>T
ENST00000676014.1:c.1912G>T	ENSP00000502058.1:p.Glu638Ter
ENST00000676035.1:n.1631G>T
ENST00000676106.1:n.2006G>T
ENST00000676137.1:n.1999G>T
ENST00000676170.1:c.2050G>T	ENSP00000502177.1:p.Glu684Ter
ENST00000676318.1:c.*2799G>T	ENSP00000502300.1:n.*2799G>T
ENST00000676336.1:c.*582G>T	ENSP00000502686.1:n.*582G>T
ENST00000676349.1:c.*1657G>T	ENSP00000502155.1:n.*1657G>T
ENST00000676399.1:n.1872G>T
ENST00000676409.1:n.2029G>T
ENST00000300417.10:c.1969G>T	ENSP00000300417.6:p.Glu657Ter
ENST00000323301.8:c.1969G>T	ENSP00000322937.4:p.Glu657Ter
ENST00000373322.1:c.1969G>T	ENSP00000362419.1:p.Glu657Ter
ENST00000373324.8:c.1888G>T	ENSP00000362421.4:p.Glu630Ter
ENST00000483302.5:n.1191G>T
NM_001005373.3:c.1969G>T	NP_001005373.1:p.Glu657Ter
NM_001005374.3:c.1969G>T	NP_001005374.1:p.Glu657Ter
NM_001190723.2:c.1888G>T	NP_001177652.1:p.Glu630Ter
NM_138361.5:c.1969G>T , LRG_373t1:c.1969G>T	NP_612370.3:p.Glu657Ter
XM_006717316.2:c.1870G>T	XP_006717379.1:p.Glu624Ter
XM_006717316.4:c.1870G>T	XP_006717379.1:p.Glu624Ter
XM_017015283.1:c.1969G>T	XP_016870772.1:p.Glu657Ter
XM_017015284.2:c.1180G>T	XP_016870773.1:p.Glu394Ter
XR_001746415.2:n.2504G>T
XR_929874.3:n.2328G>T
NM_001190723.3:c.1888G>T	NP_001177652.1:p.Glu630Ter
NM_001005373.4:c.1969G>T MANE Select	NP_001005373.1:p.Glu657Ter
NM_001005374.4:c.1969G>T	NP_001005374.1:p.Glu657Ter
NM_001384142.1:c.1969G>T	NP_001371071.1:p.Glu657Ter
NM_001384143.1:c.1870G>T	NP_001371072.1:p.Glu624Ter
NM_001384144.1:c.1180G>T	NP_001371073.1:p.Glu394Ter
NR_168891.1:n.2498G>T
NR_168892.1:n.2322G>T