Canonical Allele Identifier: CA374938148

Gene: LRSAM1

Linked Data

• MyVariant Identifiers: chr9:g.130263305G>T (hg19) ; chr9:g.127501026G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127501026G>T , CM000671.2:g.127501026G>T	GRCh38
NC_000009.11:g.130263305G>T , CM000671.1:g.130263305G>T	GRCh37
NC_000009.10:g.129303126G>T	NCBI36
NG_032008.1:g.54541G>T , LRG_373:g.54541G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300417.11:c.1929G>T MANE Select	ENSP00000300417.6:p.Met643Ile
ENST00000472068.2:c.*1653G>T	ENSP00000501555.1:n.*1653G>T
ENST00000483302.6:n.2594G>T
ENST00000498513.6:c.*820G>T	ENSP00000501637.1:n.*820G>T
ENST00000674511.1:n.1528G>T
ENST00000674516.1:c.*545G>T	ENSP00000502441.1:n.*545G>T
ENST00000674621.1:n.1861-2347G>T
ENST00000674771.1:c.*572G>T	ENSP00000502627.1:n.*572G>T
ENST00000674784.1:c.*989G>T	ENSP00000501837.1:n.*989G>T
ENST00000674970.1:c.*1703G>T	ENSP00000502493.1:n.*1703G>T
ENST00000675012.1:n.1873G>T
ENST00000675141.1:c.1830G>T	ENSP00000502420.1:p.Met610Ile
ENST00000675198.1:n.1809G>T
ENST00000675213.1:c.1884G>T	ENSP00000502218.1:p.Met628Ile
ENST00000675224.1:c.1957G>T	ENSP00000501869.1:p.Gly653Trp
ENST00000675253.1:c.*601G>T	ENSP00000502557.1:n.*601G>T
ENST00000675445.1:c.*1601G>T	ENSP00000502253.1:n.*1601G>T
ENST00000675448.1:c.1929G>T	ENSP00000502167.1:p.Met643Ile
ENST00000675521.1:n.1839G>T
ENST00000675572.1:c.1830G>T	ENSP00000501598.1:p.Met610Ile
ENST00000675641.1:c.*671G>T	ENSP00000501845.1:n.*671G>T
ENST00000675657.1:c.*542G>T	ENSP00000502002.1:n.*542G>T
ENST00000675662.1:n.1724G>T
ENST00000675789.1:c.1749G>T	ENSP00000501954.1:p.Met583Ile
ENST00000675883.1:c.1848G>T	ENSP00000501592.1:p.Met616Ile
ENST00000675945.1:c.*570G>T	ENSP00000501835.1:n.*570G>T
ENST00000676014.1:c.1872G>T	ENSP00000502058.1:p.Met624Ile
ENST00000676035.1:n.1591G>T
ENST00000676106.1:n.1966G>T
ENST00000676137.1:n.1959G>T
ENST00000676170.1:c.2010G>T	ENSP00000502177.1:p.Met670Ile
ENST00000676318.1:c.*2759G>T	ENSP00000502300.1:n.*2759G>T
ENST00000676336.1:c.*542G>T	ENSP00000502686.1:n.*542G>T
ENST00000676349.1:c.*1617G>T	ENSP00000502155.1:n.*1617G>T
ENST00000676399.1:n.1832G>T
ENST00000676409.1:n.1989G>T
ENST00000300417.10:c.1929G>T	ENSP00000300417.6:p.Met643Ile
ENST00000323301.8:c.1929G>T	ENSP00000322937.4:p.Met643Ile
ENST00000373322.1:c.1929G>T	ENSP00000362419.1:p.Met643Ile
ENST00000373324.8:c.1848G>T	ENSP00000362421.4:p.Met616Ile
ENST00000472068.1:n.822G>T
ENST00000483302.5:n.1151G>T
NM_001005373.3:c.1929G>T	NP_001005373.1:p.Met643Ile
NM_001005374.3:c.1929G>T	NP_001005374.1:p.Met643Ile
NM_001190723.2:c.1848G>T	NP_001177652.1:p.Met616Ile
NM_138361.5:c.1929G>T , LRG_373t1:c.1929G>T	NP_612370.3:p.Met643Ile
XM_006717316.2:c.1830G>T	XP_006717379.1:p.Met610Ile
XM_006717316.4:c.1830G>T	XP_006717379.1:p.Met610Ile
XM_017015283.1:c.1929G>T	XP_016870772.1:p.Met643Ile
XM_017015284.2:c.1140G>T	XP_016870773.1:p.Met380Ile
XR_001746415.2:n.2464G>T
XR_929874.3:n.2288G>T
NM_001190723.3:c.1848G>T	NP_001177652.1:p.Met616Ile
NM_001005373.4:c.1929G>T MANE Select	NP_001005373.1:p.Met643Ile
NM_001005374.4:c.1929G>T	NP_001005374.1:p.Met643Ile
NM_001384142.1:c.1929G>T	NP_001371071.1:p.Met643Ile
NM_001384143.1:c.1830G>T	NP_001371072.1:p.Met610Ile
NM_001384144.1:c.1140G>T	NP_001371073.1:p.Met380Ile
NR_168891.1:n.2458G>T
NR_168892.1:n.2282G>T