Canonical Allele Identifier: CA374938173

Gene: LRSAM1

Linked Data

• MyVariant Identifiers: chr9:g.130263318A>T (hg19) ; chr9:g.127501039A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127501039A>T , CM000671.2:g.127501039A>T	GRCh38
NC_000009.11:g.130263318A>T , CM000671.1:g.130263318A>T	GRCh37
NC_000009.10:g.129303139A>T	NCBI36
NG_032008.1:g.54554A>T , LRG_373:g.54554A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300417.11:c.1942A>T MANE Select	ENSP00000300417.6:p.Thr648Ser
ENST00000472068.2:c.*1666A>T	ENSP00000501555.1:n.*1666A>T
ENST00000483302.6:n.2607A>T
ENST00000498513.6:c.*833A>T	ENSP00000501637.1:n.*833A>T
ENST00000674511.1:n.1541A>T
ENST00000674516.1:c.*558A>T	ENSP00000502441.1:n.*558A>T
ENST00000674621.1:n.1861-2334A>T
ENST00000674771.1:c.*585A>T	ENSP00000502627.1:n.*585A>T
ENST00000674784.1:c.*1002A>T	ENSP00000501837.1:n.*1002A>T
ENST00000674970.1:c.*1716A>T	ENSP00000502493.1:n.*1716A>T
ENST00000675012.1:n.1886A>T
ENST00000675141.1:c.1843A>T	ENSP00000502420.1:p.Thr615Ser
ENST00000675198.1:n.1822A>T
ENST00000675213.1:c.1897A>T	ENSP00000502218.1:p.Thr633Ser
ENST00000675224.1:c.*8A>T	ENSP00000501869.1:n.*8A>T
ENST00000675253.1:c.*614A>T	ENSP00000502557.1:n.*614A>T
ENST00000675445.1:c.*1614A>T	ENSP00000502253.1:n.*1614A>T
ENST00000675448.1:c.1942A>T	ENSP00000502167.1:p.Thr648Ser
ENST00000675521.1:n.1852A>T
ENST00000675572.1:c.1843A>T	ENSP00000501598.1:p.Thr615Ser
ENST00000675641.1:c.*684A>T	ENSP00000501845.1:n.*684A>T
ENST00000675657.1:c.*555A>T	ENSP00000502002.1:n.*555A>T
ENST00000675662.1:n.1737A>T
ENST00000675789.1:c.1762A>T	ENSP00000501954.1:p.Thr588Ser
ENST00000675883.1:c.1861A>T	ENSP00000501592.1:p.Thr621Ser
ENST00000675945.1:c.*583A>T	ENSP00000501835.1:n.*583A>T
ENST00000676014.1:c.1885A>T	ENSP00000502058.1:p.Thr629Ser
ENST00000676035.1:n.1604A>T
ENST00000676106.1:n.1979A>T
ENST00000676137.1:n.1972A>T
ENST00000676170.1:c.2023A>T	ENSP00000502177.1:p.Thr675Ser
ENST00000676318.1:c.*2772A>T	ENSP00000502300.1:n.*2772A>T
ENST00000676336.1:c.*555A>T	ENSP00000502686.1:n.*555A>T
ENST00000676349.1:c.*1630A>T	ENSP00000502155.1:n.*1630A>T
ENST00000676399.1:n.1845A>T
ENST00000676409.1:n.2002A>T
ENST00000300417.10:c.1942A>T	ENSP00000300417.6:p.Thr648Ser
ENST00000323301.8:c.1942A>T	ENSP00000322937.4:p.Thr648Ser
ENST00000373322.1:c.1942A>T	ENSP00000362419.1:p.Thr648Ser
ENST00000373324.8:c.1861A>T	ENSP00000362421.4:p.Thr621Ser
ENST00000472068.1:n.835A>T
ENST00000483302.5:n.1164A>T
NM_001005373.3:c.1942A>T	NP_001005373.1:p.Thr648Ser
NM_001005374.3:c.1942A>T	NP_001005374.1:p.Thr648Ser
NM_001190723.2:c.1861A>T	NP_001177652.1:p.Thr621Ser
NM_138361.5:c.1942A>T , LRG_373t1:c.1942A>T	NP_612370.3:p.Thr648Ser
XM_006717316.2:c.1843A>T	XP_006717379.1:p.Thr615Ser
XM_006717316.4:c.1843A>T	XP_006717379.1:p.Thr615Ser
XM_017015283.1:c.1942A>T	XP_016870772.1:p.Thr648Ser
XM_017015284.2:c.1153A>T	XP_016870773.1:p.Thr385Ser
XR_001746415.2:n.2477A>T
XR_929874.3:n.2301A>T
NM_001190723.3:c.1861A>T	NP_001177652.1:p.Thr621Ser
NM_001005373.4:c.1942A>T MANE Select	NP_001005373.1:p.Thr648Ser
NM_001005374.4:c.1942A>T	NP_001005374.1:p.Thr648Ser
NM_001384142.1:c.1942A>T	NP_001371071.1:p.Thr648Ser
NM_001384143.1:c.1843A>T	NP_001371072.1:p.Thr615Ser
NM_001384144.1:c.1153A>T	NP_001371073.1:p.Thr385Ser
NR_168891.1:n.2471A>T
NR_168892.1:n.2295A>T