Canonical Allele Identifier: CA367209693

Gene: ANLN

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.36411062C>A , CM000669.2:g.36411062C>A	GRCh38
NC_000007.13:g.36450671C>A , CM000669.1:g.36450671C>A	GRCh37
NC_000007.12:g.36417196C>A	NCBI36
NG_041770.1:g.26260C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265748.7:c.1291C>A MANE Select	ENSP00000265748.2:p.Arg431Ser
ENST00000265748.6:c.1291C>A	ENSP00000265748.2:p.Arg431Ser
ENST00000396068.6:c.1291C>A	ENSP00000379380.2:p.Arg431Ser
ENST00000428612.5:c.96+407C>A
ENST00000441696.5:c.586C>A
ENST00000452877.5:c.452+358C>A
ENST00000495714.1:n.434C>A
NM_001284301.2:c.1291C>A	NP_001271230.1:p.Arg431Ser
NM_001284302.2:c.1291C>A	NP_001271231.1:p.Arg431Ser
NM_018685.4:c.1291C>A	NP_061155.2:p.Arg431Ser
XM_006715746.1:c.1291C>A	XP_006715809.1:p.Arg431Ser
XM_006715747.2:c.1291C>A	XP_006715810.1:p.Arg431Ser
XM_006715746.2:c.1291C>A	XP_006715809.1:p.Arg431Ser
XM_006715747.4:c.1291C>A	XP_006715810.1:p.Arg431Ser
XM_017012354.2:c.1291C>A	XP_016867843.1:p.Arg431Ser
XM_017012355.2:c.1291C>A	XP_016867844.1:p.Arg431Ser
XM_017012356.2:c.1291C>A	XP_016867845.1:p.Arg431Ser
NM_018685.5:c.1291C>A MANE Select	NP_061155.2:p.Arg431Ser
NM_001284301.3:c.1291C>A	NP_001271230.1:p.Arg431Ser
NM_001284302.3:c.1291C>A	NP_001271231.1:p.Arg431Ser