Canonical Allele Identifier: CA4219670

Gene: ANLN

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.36419219G>A , CM000669.2:g.36419219G>A	GRCh38
NC_000007.13:g.36458828G>A , CM000669.1:g.36458828G>A	GRCh37
NC_000007.12:g.36425353G>A	NCBI36
NG_041770.1:g.34417G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_018685.5:c.1634-25G>A MANE Select	NP_061155.2:n.1634-25G>A
ENST00000265748.7:c.1634-25G>A MANE Select	ENSP00000265748.2:n.1634-25G>A
NM_001284301.2:c.1523-25G>A	NP_001271230.1:n.1523-25G>A
NM_001284301.3:c.1523-25G>A	NP_001271230.1:n.1523-25G>A
NM_001284302.2:c.1523-28G>A	NP_001271231.1:n.1523-28G>A
NM_001284302.3:c.1523-28G>A	NP_001271231.1:n.1523-28G>A
NM_018685.4:c.1634-25G>A	NP_061155.2:n.1634-25G>A
ENST00000265748.6:c.1634-25G>A	ENSP00000265748.2:n.1634-25G>A
ENST00000396068.6:c.1523-25G>A	ENSP00000379380.2:n.1523-25G>A
ENST00000428612.5:c.97-5326G>A
XM_006715746.1:c.1634-25G>A	XP_006715809.1:n.1634-25G>A
XM_006715746.2:c.1634-25G>A	XP_006715809.1:n.1634-25G>A
XM_006715747.2:c.1523-25G>A	XP_006715810.1:n.1523-25G>A
XM_006715747.4:c.1523-25G>A	XP_006715810.1:n.1523-25G>A
XM_017012354.2:c.1634-25G>A	XP_016867843.1:n.1634-25G>A
XM_017012355.2:c.1634-25G>A	XP_016867844.1:n.1634-25G>A
XM_017012356.2:c.1523-25G>A	XP_016867845.1:n.1523-25G>A