Canonical Allele Identifier: CA4219852

Gene: ANLN

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.36422718T>A , CM000669.2:g.36422718T>A	GRCh38
NC_000007.13:g.36462327T>A , CM000669.1:g.36462327T>A	GRCh37
NC_000007.12:g.36428852T>A	NCBI36
NG_041770.1:g.37916T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_018685.5:c.2385T>A MANE Select	NP_061155.2:p.Ser795Arg
ENST00000265748.7:c.2385T>A MANE Select	ENSP00000265748.2:p.Ser795Arg
NM_001284301.2:c.2274T>A	NP_001271230.1:p.Ser758Arg
NM_001284301.3:c.2274T>A	NP_001271230.1:p.Ser758Arg
NM_001284302.2:c.2271T>A	NP_001271231.1:p.Ser757Arg
NM_001284302.3:c.2271T>A	NP_001271231.1:p.Ser757Arg
NM_018685.4:c.2385T>A	NP_061155.2:p.Ser795Arg
ENST00000265748.6:c.2385T>A	ENSP00000265748.2:p.Ser795Arg
ENST00000396068.6:c.2274T>A	ENSP00000379380.2:p.Ser758Arg
ENST00000428612.5:c.97-1827T>A
ENST00000446635.5:c.446T>A
XM_006715746.1:c.2385T>A	XP_006715809.1:p.Ser795Arg
XM_006715746.2:c.2385T>A	XP_006715809.1:p.Ser795Arg
XM_006715747.2:c.2274T>A	XP_006715810.1:p.Ser758Arg
XM_006715747.4:c.2274T>A	XP_006715810.1:p.Ser758Arg
XM_017012354.2:c.2373T>A	XP_016867843.1:p.Ser791Arg
XM_017012355.2:c.2373T>A	XP_016867844.1:p.Ser791Arg
XM_017012356.2:c.2262T>A	XP_016867845.1:p.Ser754Arg