Canonical Allele Identifier: CA4220104

Gene: ANLN

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.36449744G>A , CM000669.2:g.36449744G>A	GRCh38
NC_000007.13:g.36489353G>A , CM000669.1:g.36489353G>A	GRCh37
NC_000007.12:g.36455878G>A	NCBI36
NG_041770.1:g.64942G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_018685.5:c.3158G>A MANE Select	NP_061155.2:p.Arg1053His
ENST00000265748.7:c.3158G>A MANE Select	ENSP00000265748.2:p.Arg1053His
NM_001284301.2:c.3047G>A	NP_001271230.1:p.Arg1016His
NM_001284301.3:c.3047G>A	NP_001271230.1:p.Arg1016His
NM_001284302.2:c.3044G>A	NP_001271231.1:p.Arg1015His
NM_001284302.3:c.3044G>A	NP_001271231.1:p.Arg1015His
NM_018685.4:c.3158G>A	NP_061155.2:p.Arg1053His
ENST00000265748.6:c.3158G>A	ENSP00000265748.2:p.Arg1053His
ENST00000396068.6:c.3047G>A	ENSP00000379380.2:p.Arg1016His
ENST00000428612.5:c.651G>A
ENST00000491782.1:n.806G>A
XM_006715746.1:c.3212G>A	XP_006715809.1:p.Arg1071His
XM_006715746.2:c.3212G>A	XP_006715809.1:p.Arg1071His
XM_006715747.2:c.3101G>A	XP_006715810.1:p.Arg1034His
XM_006715747.4:c.3101G>A	XP_006715810.1:p.Arg1034His
XM_017012354.2:c.3200G>A	XP_016867843.1:p.Arg1067His
XM_017012355.2:c.3146G>A	XP_016867844.1:p.Arg1049His
XM_017012356.2:c.3035G>A	XP_016867845.1:p.Arg1012His