Canonical Allele Identifier: CA2355967049

Gene: CST3

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.23637624T= , CM000682.2:g.23637624T=	GRCh38
NC_000020.10:g.23618261T= , CM000682.1:g.23618261T=	GRCh37
NC_000020.9:g.23566261T=	NCBI36
NG_012887.2:g.5314A=
NG_012887.3:g.5314A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376925.8:c.239A= MANE Select	ENSP00000366124.3:p.Lys80=
ENST00000376925.7:c.239A=	ENSP00000366124.3:p.Lys80=
ENST00000398409.1:c.239A=	ENSP00000381446.1:p.Lys80=
ENST00000398411.5:c.239A=	ENSP00000381448.1:p.Lys80=
NM_000099.3:c.239A=	NP_000090.1:p.Lys80=
NM_001288614.1:c.239A=	NP_001275543.1:p.Lys80=
NM_000099.4:c.239A= MANE Select	NP_000090.1:p.Lys80=
NM_001288614.2:c.239A=	NP_001275543.1:p.Lys80=