Canonical Allele Identifier: CA374938253

Gene: LRSAM1

Linked Data

• MyVariant Identifiers: chr9:g.130263358C>T (hg19) ; chr9:g.127501079C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127501079C>T , CM000671.2:g.127501079C>T	GRCh38
NC_000009.11:g.130263358C>T , CM000671.1:g.130263358C>T	GRCh37
NC_000009.10:g.129303179C>T	NCBI36
NG_032008.1:g.54594C>T , LRG_373:g.54594C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300417.11:c.1982C>T MANE Select	ENSP00000300417.6:p.Pro661Leu
ENST00000472068.2:c.*1706C>T	ENSP00000501555.1:n.*1706C>T
ENST00000483302.6:n.2647C>T
ENST00000498513.6:c.*873C>T	ENSP00000501637.1:n.*873C>T
ENST00000674511.1:n.1581C>T
ENST00000674516.1:c.*598C>T	ENSP00000502441.1:n.*598C>T
ENST00000674621.1:n.1861-2294C>T
ENST00000674771.1:c.*625C>T	ENSP00000502627.1:n.*625C>T
ENST00000674784.1:c.*1042C>T	ENSP00000501837.1:n.*1042C>T
ENST00000674970.1:c.*1756C>T	ENSP00000502493.1:n.*1756C>T
ENST00000675012.1:n.1926C>T
ENST00000675141.1:c.1883C>T	ENSP00000502420.1:p.Pro628Leu
ENST00000675198.1:n.1862C>T
ENST00000675213.1:c.1937C>T	ENSP00000502218.1:p.Pro646Leu
ENST00000675224.1:c.*48C>T	ENSP00000501869.1:n.*48C>T
ENST00000675253.1:c.*654C>T	ENSP00000502557.1:n.*654C>T
ENST00000675445.1:c.*1654C>T	ENSP00000502253.1:n.*1654C>T
ENST00000675448.1:c.1982C>T	ENSP00000502167.1:p.Pro661Leu
ENST00000675521.1:n.1892C>T
ENST00000675572.1:c.1883C>T	ENSP00000501598.1:p.Pro628Leu
ENST00000675641.1:c.*724C>T	ENSP00000501845.1:n.*724C>T
ENST00000675657.1:c.*595C>T	ENSP00000502002.1:n.*595C>T
ENST00000675662.1:n.1777C>T
ENST00000675789.1:c.1802C>T	ENSP00000501954.1:p.Pro601Leu
ENST00000675883.1:c.1901C>T	ENSP00000501592.1:p.Pro634Leu
ENST00000675945.1:c.*623C>T	ENSP00000501835.1:n.*623C>T
ENST00000676014.1:c.1925C>T	ENSP00000502058.1:p.Pro642Leu
ENST00000676035.1:n.1644C>T
ENST00000676106.1:n.2019C>T
ENST00000676137.1:n.2012C>T
ENST00000676170.1:c.2063C>T	ENSP00000502177.1:p.Pro688Leu
ENST00000676318.1:c.*2812C>T	ENSP00000502300.1:n.*2812C>T
ENST00000676336.1:c.*595C>T	ENSP00000502686.1:n.*595C>T
ENST00000676349.1:c.*1670C>T	ENSP00000502155.1:n.*1670C>T
ENST00000676399.1:n.1885C>T
ENST00000676409.1:n.2042C>T
ENST00000300417.10:c.1982C>T	ENSP00000300417.6:p.Pro661Leu
ENST00000323301.8:c.1982C>T	ENSP00000322937.4:p.Pro661Leu
ENST00000373322.1:c.1982C>T	ENSP00000362419.1:p.Pro661Leu
ENST00000373324.8:c.1901C>T	ENSP00000362421.4:p.Pro634Leu
ENST00000483302.5:n.1204C>T
NM_001005373.3:c.1982C>T	NP_001005373.1:p.Pro661Leu
NM_001005374.3:c.1982C>T	NP_001005374.1:p.Pro661Leu
NM_001190723.2:c.1901C>T	NP_001177652.1:p.Pro634Leu
NM_138361.5:c.1982C>T , LRG_373t1:c.1982C>T	NP_612370.3:p.Pro661Leu
XM_006717316.2:c.1883C>T	XP_006717379.1:p.Pro628Leu
XM_006717316.4:c.1883C>T	XP_006717379.1:p.Pro628Leu
XM_017015283.1:c.1982C>T	XP_016870772.1:p.Pro661Leu
XM_017015284.2:c.1193C>T	XP_016870773.1:p.Pro398Leu
XR_001746415.2:n.2517C>T
XR_929874.3:n.2341C>T
NM_001190723.3:c.1901C>T	NP_001177652.1:p.Pro634Leu
NM_001005373.4:c.1982C>T MANE Select	NP_001005373.1:p.Pro661Leu
NM_001005374.4:c.1982C>T	NP_001005374.1:p.Pro661Leu
NM_001384142.1:c.1982C>T	NP_001371071.1:p.Pro661Leu
NM_001384143.1:c.1883C>T	NP_001371072.1:p.Pro628Leu
NM_001384144.1:c.1193C>T	NP_001371073.1:p.Pro398Leu
NR_168891.1:n.2511C>T
NR_168892.1:n.2335C>T