Canonical Allele Identifier: CA374938273

Gene: LRSAM1

Linked Data

• MyVariant Identifiers: chr9:g.130263372G>T (hg19) ; chr9:g.127501093G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127501093G>T , CM000671.2:g.127501093G>T	GRCh38
NC_000009.11:g.130263372G>T , CM000671.1:g.130263372G>T	GRCh37
NC_000009.10:g.129303193G>T	NCBI36
NG_032008.1:g.54608G>T , LRG_373:g.54608G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300417.11:c.1996G>T MANE Select	ENSP00000300417.6:p.Ala666Ser
ENST00000472068.2:c.*1720G>T	ENSP00000501555.1:n.*1720G>T
ENST00000483302.6:n.2661G>T
ENST00000498513.6:c.*887G>T	ENSP00000501637.1:n.*887G>T
ENST00000674511.1:n.1595G>T
ENST00000674516.1:c.*612G>T	ENSP00000502441.1:n.*612G>T
ENST00000674621.1:n.1861-2280G>T
ENST00000674771.1:c.*639G>T	ENSP00000502627.1:n.*639G>T
ENST00000674784.1:c.*1056G>T	ENSP00000501837.1:n.*1056G>T
ENST00000674970.1:c.*1770G>T	ENSP00000502493.1:n.*1770G>T
ENST00000675012.1:n.1940G>T
ENST00000675141.1:c.1897G>T	ENSP00000502420.1:p.Ala633Ser
ENST00000675198.1:n.1876G>T
ENST00000675213.1:c.1951G>T	ENSP00000502218.1:p.Ala651Ser
ENST00000675224.1:c.*62G>T	ENSP00000501869.1:n.*62G>T
ENST00000675253.1:c.*668G>T	ENSP00000502557.1:n.*668G>T
ENST00000675445.1:c.*1668G>T	ENSP00000502253.1:n.*1668G>T
ENST00000675448.1:c.1996G>T	ENSP00000502167.1:p.Ala666Ser
ENST00000675521.1:n.1906G>T
ENST00000675572.1:c.1897G>T	ENSP00000501598.1:p.Ala633Ser
ENST00000675641.1:c.*738G>T	ENSP00000501845.1:n.*738G>T
ENST00000675657.1:c.*609G>T	ENSP00000502002.1:n.*609G>T
ENST00000675662.1:n.1791G>T
ENST00000675789.1:c.1816G>T	ENSP00000501954.1:p.Ala606Ser
ENST00000675883.1:c.1915G>T	ENSP00000501592.1:p.Ala639Ser
ENST00000675945.1:c.*637G>T	ENSP00000501835.1:n.*637G>T
ENST00000676014.1:c.1939G>T	ENSP00000502058.1:p.Ala647Ser
ENST00000676035.1:n.1658G>T
ENST00000676106.1:n.2033G>T
ENST00000676137.1:n.2026G>T
ENST00000676170.1:c.2077G>T	ENSP00000502177.1:p.Ala693Ser
ENST00000676318.1:c.*2826G>T	ENSP00000502300.1:n.*2826G>T
ENST00000676336.1:c.*609G>T	ENSP00000502686.1:n.*609G>T
ENST00000676349.1:c.*1684G>T	ENSP00000502155.1:n.*1684G>T
ENST00000676399.1:n.1899G>T
ENST00000676409.1:n.2056G>T
ENST00000300417.10:c.1996G>T	ENSP00000300417.6:p.Ala666Ser
ENST00000323301.8:c.1996G>T	ENSP00000322937.4:p.Ala666Ser
ENST00000373322.1:c.1996G>T	ENSP00000362419.1:p.Ala666Ser
ENST00000373324.8:c.1915G>T	ENSP00000362421.4:p.Ala639Ser
ENST00000483302.5:n.1218G>T
NM_001005373.3:c.1996G>T	NP_001005373.1:p.Ala666Ser
NM_001005374.3:c.1996G>T	NP_001005374.1:p.Ala666Ser
NM_001190723.2:c.1915G>T	NP_001177652.1:p.Ala639Ser
NM_138361.5:c.1996G>T , LRG_373t1:c.1996G>T	NP_612370.3:p.Ala666Ser
XM_006717316.2:c.1897G>T	XP_006717379.1:p.Ala633Ser
XM_006717316.4:c.1897G>T	XP_006717379.1:p.Ala633Ser
XM_017015283.1:c.1996G>T	XP_016870772.1:p.Ala666Ser
XM_017015284.2:c.1207G>T	XP_016870773.1:p.Ala403Ser
XR_001746415.2:n.2531G>T
XR_929874.3:n.2355G>T
NM_001190723.3:c.1915G>T	NP_001177652.1:p.Ala639Ser
NM_001005373.4:c.1996G>T MANE Select	NP_001005373.1:p.Ala666Ser
NM_001005374.4:c.1996G>T	NP_001005374.1:p.Ala666Ser
NM_001384142.1:c.1996G>T	NP_001371071.1:p.Ala666Ser
NM_001384143.1:c.1897G>T	NP_001371072.1:p.Ala633Ser
NM_001384144.1:c.1207G>T	NP_001371073.1:p.Ala403Ser
NR_168891.1:n.2525G>T
NR_168892.1:n.2349G>T