Canonical Allele Identifier: CA1700121184

Gene: ANLN

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265748.7:c.1291C= MANE Select	ENSP00000265748.2:p.Arg431=
ENST00000265748.6:c.1291C=	ENSP00000265748.2:p.Arg431=
ENST00000396068.6:c.1291C=	ENSP00000379380.2:p.Arg431=
ENST00000428612.5:c.96+407C=
ENST00000441696.5:c.586C=
ENST00000452877.5:c.452+358C=
ENST00000495714.1:n.434C=
NM_001284301.2:c.1291C=	NP_001271230.1:p.Arg431=
NM_001284302.2:c.1291C=	NP_001271231.1:p.Arg431=
NM_018685.4:c.1291C=	NP_061155.2:p.Arg431=
XM_006715746.1:c.1291C=	XP_006715809.1:p.Arg431=
XM_006715747.2:c.1291C=	XP_006715810.1:p.Arg431=
XM_006715746.2:c.1291C=	XP_006715809.1:p.Arg431=
XM_006715747.4:c.1291C=	XP_006715810.1:p.Arg431=
XM_017012354.2:c.1291C=	XP_016867843.1:p.Arg431=
XM_017012355.2:c.1291C=	XP_016867844.1:p.Arg431=
XM_017012356.2:c.1291C=	XP_016867845.1:p.Arg431=
NM_018685.5:c.1291C= MANE Select	NP_061155.2:p.Arg431=
NM_001284301.3:c.1291C=	NP_001271230.1:p.Arg431=
NM_001284302.3:c.1291C=	NP_001271231.1:p.Arg431=