Canonical Allele Identifier: CA1278193559

Gene: LIMS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108558021A= , CM000664.2:g.108558021A=	GRCh38
NC_000002.11:g.109174477A= , CM000664.1:g.109174477A=	GRCh37
NC_000002.10:g.108540909A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000544547.6:c.32+23427A= MANE Select	ENSP00000437912.1:n.32+23427A=
ENST00000695516.1:c.59+24213A=	ENSP00000511979.1:n.59+24213A=
ENST00000695517.1:c.32+23427A=	ENSP00000511980.1:n.32+23427A=
ENST00000428064.5:c.32+23427A=	ENSP00000390862.1:n.32+23427A=
ENST00000544547.5:c.32+23427A=	ENSP00000437912.1:n.32+23427A=
NM_001193483.2:c.32+23427A=	NP_001180412.1:n.32+23427A=
XM_005263949.1:c.32+23427A=	XP_005264006.1:n.32+23427A=
XM_017004092.1:c.-84+23427A=	XP_016859581.1:n.-84+23427A=
NM_001193483.3:c.32+23427A= MANE Select	NP_001180412.1:n.32+23427A=
NM_001371495.1:c.32+23427A=	NP_001358424.1:n.32+23427A=
NM_001371496.1:c.59+24213A=	NP_001358425.1:n.59+24213A=
NM_001394896.1:c.32+23427A=	NP_001381825.1:n.32+23427A=
NM_001394898.1:c.59+24213A=	NP_001381827.1:n.59+24213A=