Canonical Allele Identifier: CA374931968

Gene: LRSAM1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127482949G>C , CM000671.2:g.127482949G>C	GRCh38
NC_000009.11:g.130245228G>C , CM000671.1:g.130245228G>C	GRCh37
NC_000009.10:g.129285049G>C	NCBI36
NG_032008.1:g.36464G>C , LRG_373:g.36464G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001005373.4:c.1089-1G>C MANE Select	NP_001005373.1:n.1089-1G>C
ENST00000300417.11:c.1089-1G>C MANE Select	ENSP00000300417.6:n.1089-1G>C
NM_001005373.3:c.1089-1G>C	NP_001005373.1:n.1089-1G>C
NM_001005374.3:c.1089-1G>C	NP_001005374.1:n.1089-1G>C
NM_001005374.4:c.1089-1G>C	NP_001005374.1:n.1089-1G>C
NM_001190723.2:c.1089-1G>C	NP_001177652.1:n.1089-1G>C
NM_001190723.3:c.1089-1G>C	NP_001177652.1:n.1089-1G>C
NM_001384142.1:c.1089-1G>C	NP_001371071.1:n.1089-1G>C
NM_001384143.1:c.1089-1G>C	NP_001371072.1:n.1089-1G>C
NM_001384144.1:c.300-1G>C	NP_001371073.1:n.300-1G>C
NM_138361.5:c.1089-1G>C , LRG_373t1:c.1089-1G>C	NP_612370.3:n.1089-1G>C
NR_168891.1:n.1437-1G>C
NR_168892.1:n.1437-1G>C
ENST00000300417.10:c.1089-1G>C	ENSP00000300417.6:n.1089-1G>C
ENST00000323301.8:c.1089-1G>C	ENSP00000322937.4:n.1089-1G>C
ENST00000373322.1:c.1089-1G>C	ENSP00000362419.1:n.1089-1G>C
ENST00000373324.8:c.1089-1G>C	ENSP00000362421.4:n.1089-1G>C
ENST00000472068.1:n.76-1G>C
ENST00000472068.2:c.*812-1G>C	ENSP00000501555.1:n.*812-1G>C
ENST00000483302.5:n.306-1G>C
ENST00000498513.5:n.342-1G>C
ENST00000498513.6:c.342-1G>C	ENSP00000501637.1:n.342-1G>C
ENST00000674511.1:n.964-1G>C
ENST00000674516.1:c.1089-1G>C	ENSP00000502441.1:n.1089-1G>C
ENST00000674621.1:n.995-1G>C
ENST00000674771.1:c.1089-1G>C	ENSP00000502627.1:n.1089-1G>C
ENST00000674784.1:c.*318+1722G>C	ENSP00000501837.1:n.*318+1722G>C
ENST00000674970.1:c.*863-1G>C	ENSP00000502493.1:n.*863-1G>C
ENST00000675012.1:n.969-1G>C
ENST00000675141.1:c.1089-1G>C	ENSP00000502420.1:n.1089-1G>C
ENST00000675198.1:n.991-1G>C
ENST00000675213.1:c.1044-1G>C	ENSP00000502218.1:n.1044-1G>C
ENST00000675224.1:c.1089-1G>C	ENSP00000501869.1:n.1089-1G>C
ENST00000675253.1:c.1089-1G>C	ENSP00000502557.1:n.1089-1G>C
ENST00000675445.1:c.*761-1G>C	ENSP00000502253.1:n.*761-1G>C
ENST00000675448.1:c.1089-1G>C	ENSP00000502167.1:n.1089-1G>C
ENST00000675521.1:n.941-1G>C
ENST00000675572.1:c.1089-1G>C	ENSP00000501598.1:n.1089-1G>C
ENST00000675641.1:c.1089-1G>C	ENSP00000501845.1:n.1089-1G>C
ENST00000675657.1:c.1089-1G>C	ENSP00000502002.1:n.1089-1G>C
ENST00000675662.1:n.982-1G>C
ENST00000675789.1:c.1089-1G>C	ENSP00000501954.1:n.1089-1G>C
ENST00000675883.1:c.1089-1G>C	ENSP00000501592.1:n.1089-1G>C
ENST00000675945.1:c.1089-1G>C	ENSP00000501835.1:n.1089-1G>C
ENST00000676014.1:c.1032-1G>C	ENSP00000502058.1:n.1032-1G>C
ENST00000676035.1:n.850-1G>C
ENST00000676106.1:n.894-1G>C
ENST00000676137.1:n.980-1G>C
ENST00000676170.1:c.1170-1G>C	ENSP00000502177.1:n.1170-1G>C
ENST00000676318.1:c.1089-1G>C	ENSP00000502300.1:n.1089-1G>C
ENST00000676336.1:c.867-1G>C	ENSP00000502686.1:n.867-1G>C
ENST00000676349.1:c.*858-1G>C	ENSP00000502155.1:n.*858-1G>C
ENST00000676399.1:n.987-1G>C
ENST00000676409.1:n.968-1G>C
XM_006717316.2:c.1089-1G>C	XP_006717379.1:n.1089-1G>C
XM_006717316.4:c.1089-1G>C	XP_006717379.1:n.1089-1G>C
XM_017015283.1:c.1089-1G>C	XP_016870772.1:n.1089-1G>C
XM_017015284.2:c.300-1G>C	XP_016870773.1:n.300-1G>C
XR_001746415.2:n.1443-1G>C
XR_929874.1:n.1461-1G>C
XR_929874.3:n.1443-1G>C