Canonical Allele Identifier: CA374931349

Gene: LRSAM1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127479506G>T , CM000671.2:g.127479506G>T	GRCh38
NC_000009.11:g.130241785G>T , CM000671.1:g.130241785G>T	GRCh37
NC_000009.10:g.129281606G>T	NCBI36
NG_032008.1:g.33021G>T , LRG_373:g.33021G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001005373.4:c.903+1G>T MANE Select	NP_001005373.1:n.903+1G>T
ENST00000300417.11:c.903+1G>T MANE Select	ENSP00000300417.6:n.903+1G>T
NM_001005373.3:c.903+1G>T	NP_001005373.1:n.903+1G>T
NM_001005374.3:c.903+1G>T	NP_001005374.1:n.903+1G>T
NM_001005374.4:c.903+1G>T	NP_001005374.1:n.903+1G>T
NM_001190723.2:c.903+1G>T	NP_001177652.1:n.903+1G>T
NM_001190723.3:c.903+1G>T	NP_001177652.1:n.903+1G>T
NM_001384142.1:c.903+1G>T	NP_001371071.1:n.903+1G>T
NM_001384143.1:c.903+1G>T	NP_001371072.1:n.903+1G>T
NM_001384144.1:c.114+1G>T	NP_001371073.1:n.114+1G>T
NM_138361.5:c.903+1G>T , LRG_373t1:c.903+1G>T	NP_612370.3:n.903+1G>T
NR_168891.1:n.1251+1G>T
NR_168892.1:n.1251+1G>T
ENST00000300417.10:c.903+1G>T	ENSP00000300417.6:n.903+1G>T
ENST00000323301.8:c.903+1G>T	ENSP00000322937.4:n.903+1G>T
ENST00000373322.1:c.903+1G>T	ENSP00000362419.1:n.903+1G>T
ENST00000373324.8:c.903+1G>T	ENSP00000362421.4:n.903+1G>T
ENST00000472068.2:c.*626+1G>T	ENSP00000501555.1:n.*626+1G>T
ENST00000483302.5:n.120+1G>T
ENST00000498513.5:n.156+1G>T
ENST00000498513.6:c.156+1G>T	ENSP00000501637.1:n.156+1G>T
ENST00000674511.1:n.778+1G>T
ENST00000674516.1:c.903+1G>T	ENSP00000502441.1:n.903+1G>T
ENST00000674621.1:n.809+1G>T
ENST00000674771.1:c.903+1G>T	ENSP00000502627.1:n.903+1G>T
ENST00000674784.1:c.*133+1G>T	ENSP00000501837.1:n.*133+1G>T
ENST00000674970.1:c.*677+1G>T	ENSP00000502493.1:n.*677+1G>T
ENST00000675012.1:n.783+1G>T
ENST00000675141.1:c.903+1G>T	ENSP00000502420.1:n.903+1G>T
ENST00000675198.1:n.805+1G>T
ENST00000675213.1:c.858+1G>T	ENSP00000502218.1:n.858+1G>T
ENST00000675224.1:c.903+1G>T	ENSP00000501869.1:n.903+1G>T
ENST00000675253.1:c.903+1G>T	ENSP00000502557.1:n.903+1G>T
ENST00000675445.1:c.*575+1G>T	ENSP00000502253.1:n.*575+1G>T
ENST00000675448.1:c.903+1G>T	ENSP00000502167.1:n.903+1G>T
ENST00000675521.1:n.755+1G>T
ENST00000675572.1:c.903+1G>T	ENSP00000501598.1:n.903+1G>T
ENST00000675641.1:c.903+1G>T	ENSP00000501845.1:n.903+1G>T
ENST00000675657.1:c.903+1G>T	ENSP00000502002.1:n.903+1G>T
ENST00000675662.1:n.796+1G>T
ENST00000675789.1:c.903+1G>T	ENSP00000501954.1:n.903+1G>T
ENST00000675883.1:c.903+1G>T	ENSP00000501592.1:n.903+1G>T
ENST00000675945.1:c.903+1G>T	ENSP00000501835.1:n.903+1G>T
ENST00000676014.1:c.846+1G>T	ENSP00000502058.1:n.846+1G>T
ENST00000676035.1:n.664+1G>T
ENST00000676106.1:n.708+1G>T
ENST00000676137.1:n.794+1G>T
ENST00000676170.1:c.903+1G>T	ENSP00000502177.1:n.903+1G>T
ENST00000676318.1:c.903+1G>T	ENSP00000502300.1:n.903+1G>T
ENST00000676336.1:c.681+1G>T	ENSP00000502686.1:n.681+1G>T
ENST00000676349.1:c.*672+1G>T	ENSP00000502155.1:n.*672+1G>T
ENST00000676399.1:n.801+1G>T
ENST00000676409.1:n.782+1G>T
XM_006717316.2:c.903+1G>T	XP_006717379.1:n.903+1G>T
XM_006717316.4:c.903+1G>T	XP_006717379.1:n.903+1G>T
XM_017015283.1:c.903+1G>T	XP_016870772.1:n.903+1G>T
XM_017015284.2:c.114+1G>T	XP_016870773.1:n.114+1G>T
XR_001746415.2:n.1257+1G>T
XR_929874.1:n.1275+1G>T
XR_929874.3:n.1257+1G>T