Canonical Allele Identifier: CA467237570

Gene: LRSAM1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127502842C>T , CM000671.2:g.127502842C>T	GRCh38
NC_000009.11:g.130265121C>T , CM000671.1:g.130265121C>T	GRCh37
NC_000009.10:g.129304942C>T	NCBI36
NG_032008.1:g.56357C>T , LRG_373:g.56357C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001005373.4:c.2115C>T MANE Select	NP_001005373.1:p.Thr705=
ENST00000300417.11:c.2115C>T MANE Select	ENSP00000300417.6:p.Thr705=
NM_001005373.3:c.2115C>T	NP_001005373.1:p.Thr705=
NM_001005374.3:c.2115C>T	NP_001005374.1:p.Thr705=
NM_001005374.4:c.2115C>T	NP_001005374.1:p.Thr705=
NM_001190723.2:c.2034C>T	NP_001177652.1:p.Thr678=
NM_001190723.3:c.2034C>T	NP_001177652.1:p.Thr678=
NM_001384142.1:c.2115C>T	NP_001371071.1:p.Thr705=
NM_001384143.1:c.2016C>T	NP_001371072.1:p.Thr672=
NM_001384144.1:c.1326C>T	NP_001371073.1:p.Thr442=
NM_138361.5:c.2115C>T , LRG_373t1:c.2115C>T	NP_612370.3:p.Thr705=
NR_168891.1:n.2644C>T
NR_168892.1:n.2468C>T
ENST00000300417.10:c.2115C>T	ENSP00000300417.6:p.Thr705=
ENST00000323301.8:c.2115C>T	ENSP00000322937.4:p.Thr705=
ENST00000373322.1:c.2115C>T	ENSP00000362419.1:p.Thr705=
ENST00000373324.8:c.2034C>T	ENSP00000362421.4:p.Thr678=
ENST00000483302.5:n.1337C>T
ENST00000483302.6:n.2780C>T
ENST00000498513.6:c.*1006C>T	ENSP00000501637.1:n.*1006C>T
ENST00000674511.1:n.1714C>T
ENST00000674516.1:c.*731C>T	ENSP00000502441.1:n.*731C>T
ENST00000674621.1:n.1861-531C>T
ENST00000674771.1:c.*758C>T	ENSP00000502627.1:n.*758C>T
ENST00000674784.1:c.*1175C>T	ENSP00000501837.1:n.*1175C>T
ENST00000674970.1:c.*1889C>T	ENSP00000502493.1:n.*1889C>T
ENST00000675012.1:n.2059C>T
ENST00000675141.1:c.2016C>T	ENSP00000502420.1:p.Thr672=
ENST00000675198.1:n.1995C>T
ENST00000675213.1:c.2070C>T	ENSP00000502218.1:p.Thr690=
ENST00000675224.1:c.*181C>T	ENSP00000501869.1:n.*181C>T
ENST00000675253.1:c.*787C>T	ENSP00000502557.1:n.*787C>T
ENST00000675445.1:c.*1787C>T	ENSP00000502253.1:n.*1787C>T
ENST00000675448.1:c.2115C>T	ENSP00000502167.1:p.Thr705=
ENST00000675521.1:n.2025C>T
ENST00000675572.1:c.2016C>T	ENSP00000501598.1:p.Thr672=
ENST00000675641.1:c.*857C>T	ENSP00000501845.1:n.*857C>T
ENST00000675657.1:c.*728C>T	ENSP00000502002.1:n.*728C>T
ENST00000675662.1:n.1910C>T
ENST00000675789.1:c.1935C>T	ENSP00000501954.1:p.Thr645=
ENST00000675883.1:c.2034C>T	ENSP00000501592.1:p.Thr678=
ENST00000675945.1:c.*756C>T	ENSP00000501835.1:n.*756C>T
ENST00000676014.1:c.2058C>T	ENSP00000502058.1:p.Thr686=
ENST00000676035.1:n.1777C>T
ENST00000676106.1:n.2152C>T
ENST00000676137.1:n.2145C>T
ENST00000676170.1:c.2196C>T	ENSP00000502177.1:p.Thr732=
ENST00000676318.1:c.*2945C>T	ENSP00000502300.1:n.*2945C>T
ENST00000676336.1:c.*728C>T	ENSP00000502686.1:n.*728C>T
ENST00000676349.1:c.*1803C>T	ENSP00000502155.1:n.*1803C>T
ENST00000676399.1:n.2018C>T
ENST00000676409.1:n.2175C>T
XM_006717316.2:c.2016C>T	XP_006717379.1:p.Thr672=
XM_006717316.4:c.2016C>T	XP_006717379.1:p.Thr672=
XM_017015283.1:c.2115C>T	XP_016870772.1:p.Thr705=
XM_017015284.2:c.1326C>T	XP_016870773.1:p.Thr442=
XR_001746415.2:n.2650C>T
XR_929874.3:n.2474C>T