Canonical Allele Identifier: CA1278193635

Gene: LIMS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108558222_108558226delinsCTTTT , CM000664.2:g.108558222_108558226delinsCTTTT	GRCh38
NC_000002.11:g.109174678_109174682delinsCTTTT , CM000664.1:g.109174678_109174682delinsCTTTT	GRCh37
NC_000002.10:g.108541110_108541114delinsCTTTT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000544547.6:c.32+23628_32+23632delinsCTTTT MANE Select	ENSP00000437912.1:n.32+23628_32+23632delinsCTTTT
ENST00000695516.1:c.59+24414_59+24418delinsCTTTT	ENSP00000511979.1:n.59+24414_59+24418delinsCTTTT
ENST00000695517.1:c.32+23628_32+23632delinsCTTTT	ENSP00000511980.1:n.32+23628_32+23632delinsCTTTT
ENST00000428064.5:c.32+23628_32+23632delinsCTTTT	ENSP00000390862.1:n.32+23628_32+23632delinsCTTTT
ENST00000544547.5:c.32+23628_32+23632delinsCTTTT	ENSP00000437912.1:n.32+23628_32+23632delinsCTTTT
NM_001193483.2:c.32+23628_32+23632delinsCTTTT	NP_001180412.1:n.32+23628_32+23632delinsCTTTT
XM_005263949.1:c.32+23628_32+23632delinsCTTTT	XP_005264006.1:n.32+23628_32+23632delinsCTTTT
XM_017004092.1:c.-84+23628_-84+23632delinsCTTTT	XP_016859581.1:n.-84+23628_-84+23632delinsCTTTT
NM_001193483.3:c.32+23628_32+23632delinsCTTTT MANE Select	NP_001180412.1:n.32+23628_32+23632delinsCTTTT
NM_001371495.1:c.32+23628_32+23632delinsCTTTT	NP_001358424.1:n.32+23628_32+23632delinsCTTTT
NM_001371496.1:c.59+24414_59+24418delinsCTTTT	NP_001358425.1:n.59+24414_59+24418delinsCTTTT
NM_001394896.1:c.32+23628_32+23632delinsCTTTT	NP_001381825.1:n.32+23628_32+23632delinsCTTTT
NM_001394898.1:c.59+24414_59+24418delinsCTTTT	NP_001381827.1:n.59+24414_59+24418delinsCTTTT