Canonical Allele Identifier: CA367212398

Gene: ANLN

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.36419462G>T , CM000669.2:g.36419462G>T	GRCh38
NC_000007.13:g.36459071G>T , CM000669.1:g.36459071G>T	GRCh37
NC_000007.12:g.36425596G>T	NCBI36
NG_041770.1:g.34660G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_018685.5:c.1852G>T MANE Select	NP_061155.2:p.Gly618Cys
ENST00000265748.7:c.1852G>T MANE Select	ENSP00000265748.2:p.Gly618Cys
NM_001284301.2:c.1741G>T	NP_001271230.1:p.Gly581Cys
NM_001284301.3:c.1741G>T	NP_001271230.1:p.Gly581Cys
NM_001284302.2:c.1738G>T	NP_001271231.1:p.Gly580Cys
NM_001284302.3:c.1738G>T	NP_001271231.1:p.Gly580Cys
NM_018685.4:c.1852G>T	NP_061155.2:p.Gly618Cys
ENST00000265748.6:c.1852G>T	ENSP00000265748.2:p.Gly618Cys
ENST00000396068.6:c.1741G>T	ENSP00000379380.2:p.Gly581Cys
ENST00000428612.5:c.97-5083G>T
XM_006715746.1:c.1852G>T	XP_006715809.1:p.Gly618Cys
XM_006715746.2:c.1852G>T	XP_006715809.1:p.Gly618Cys
XM_006715747.2:c.1741G>T	XP_006715810.1:p.Gly581Cys
XM_006715747.4:c.1741G>T	XP_006715810.1:p.Gly581Cys
XM_017012354.2:c.1852G>T	XP_016867843.1:p.Gly618Cys
XM_017012355.2:c.1852G>T	XP_016867844.1:p.Gly618Cys
XM_017012356.2:c.1741G>T	XP_016867845.1:p.Gly581Cys