Canonical Allele Identifier: CA467236857

Gene: LRSAM1

Linked Data

• MyVariant Identifiers: chr9:g.130263374A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127501095A>T , CM000671.2:g.127501095A>T	GRCh38
NC_000009.11:g.130263374A>T , CM000671.1:g.130263374A>T	GRCh37
NC_000009.10:g.129303195A>T	NCBI36
NG_032008.1:g.54610A>T , LRG_373:g.54610A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300417.11:c.1998A>T MANE Select	ENSP00000300417.6:p.Ala666=
ENST00000472068.2:c.*1722A>T	ENSP00000501555.1:n.*1722A>T
ENST00000483302.6:n.2663A>T
ENST00000498513.6:c.*889A>T	ENSP00000501637.1:n.*889A>T
ENST00000674511.1:n.1597A>T
ENST00000674516.1:c.*614A>T	ENSP00000502441.1:n.*614A>T
ENST00000674621.1:n.1861-2278A>T
ENST00000674771.1:c.*641A>T	ENSP00000502627.1:n.*641A>T
ENST00000674784.1:c.*1058A>T	ENSP00000501837.1:n.*1058A>T
ENST00000674970.1:c.*1772A>T	ENSP00000502493.1:n.*1772A>T
ENST00000675012.1:n.1942A>T
ENST00000675141.1:c.1899A>T	ENSP00000502420.1:p.Ala633=
ENST00000675198.1:n.1878A>T
ENST00000675213.1:c.1953A>T	ENSP00000502218.1:p.Ala651=
ENST00000675224.1:c.*64A>T	ENSP00000501869.1:n.*64A>T
ENST00000675253.1:c.*670A>T	ENSP00000502557.1:n.*670A>T
ENST00000675445.1:c.*1670A>T	ENSP00000502253.1:n.*1670A>T
ENST00000675448.1:c.1998A>T	ENSP00000502167.1:p.Ala666=
ENST00000675521.1:n.1908A>T
ENST00000675572.1:c.1899A>T	ENSP00000501598.1:p.Ala633=
ENST00000675641.1:c.*740A>T	ENSP00000501845.1:n.*740A>T
ENST00000675657.1:c.*611A>T	ENSP00000502002.1:n.*611A>T
ENST00000675662.1:n.1793A>T
ENST00000675789.1:c.1818A>T	ENSP00000501954.1:p.Ala606=
ENST00000675883.1:c.1917A>T	ENSP00000501592.1:p.Ala639=
ENST00000675945.1:c.*639A>T	ENSP00000501835.1:n.*639A>T
ENST00000676014.1:c.1941A>T	ENSP00000502058.1:p.Ala647=
ENST00000676035.1:n.1660A>T
ENST00000676106.1:n.2035A>T
ENST00000676137.1:n.2028A>T
ENST00000676170.1:c.2079A>T	ENSP00000502177.1:p.Ala693=
ENST00000676318.1:c.*2828A>T	ENSP00000502300.1:n.*2828A>T
ENST00000676336.1:c.*611A>T	ENSP00000502686.1:n.*611A>T
ENST00000676349.1:c.*1686A>T	ENSP00000502155.1:n.*1686A>T
ENST00000676399.1:n.1901A>T
ENST00000676409.1:n.2058A>T
ENST00000300417.10:c.1998A>T	ENSP00000300417.6:p.Ala666=
ENST00000323301.8:c.1998A>T	ENSP00000322937.4:p.Ala666=
ENST00000373322.1:c.1998A>T	ENSP00000362419.1:p.Ala666=
ENST00000373324.8:c.1917A>T	ENSP00000362421.4:p.Ala639=
ENST00000483302.5:n.1220A>T
NM_001005373.3:c.1998A>T	NP_001005373.1:p.Ala666=
NM_001005374.3:c.1998A>T	NP_001005374.1:p.Ala666=
NM_001190723.2:c.1917A>T	NP_001177652.1:p.Ala639=
NM_138361.5:c.1998A>T , LRG_373t1:c.1998A>T	NP_612370.3:p.Ala666=
XM_006717316.2:c.1899A>T	XP_006717379.1:p.Ala633=
XM_006717316.4:c.1899A>T	XP_006717379.1:p.Ala633=
XM_017015283.1:c.1998A>T	XP_016870772.1:p.Ala666=
XM_017015284.2:c.1209A>T	XP_016870773.1:p.Ala403=
XR_001746415.2:n.2533A>T
XR_929874.3:n.2357A>T
NM_001190723.3:c.1917A>T	NP_001177652.1:p.Ala639=
NM_001005373.4:c.1998A>T MANE Select	NP_001005373.1:p.Ala666=
NM_001005374.4:c.1998A>T	NP_001005374.1:p.Ala666=
NM_001384142.1:c.1998A>T	NP_001371071.1:p.Ala666=
NM_001384143.1:c.1899A>T	NP_001371072.1:p.Ala633=
NM_001384144.1:c.1209A>T	NP_001371073.1:p.Ala403=
NR_168891.1:n.2527A>T
NR_168892.1:n.2351A>T