Canonical Allele Identifier: CA1404304499

Gene: PCCB

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.136328787T= , CM000665.2:g.136328787T=	GRCh38
NC_000003.11:g.136047629T= , CM000665.1:g.136047629T=	GRCh37
NC_000003.10:g.137530319T=	NCBI36
NG_008939.1:g.83463T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000251654.9:c.1428T= MANE Select	ENSP00000251654.4:p.His476=
ENST00000251654.8:c.1428T=	ENSP00000251654.4:p.His476=
ENST00000462637.5:c.1359T=	ENSP00000420391.1:p.His453=
ENST00000466072.5:c.1488T=	ENSP00000420158.1:p.His496=
ENST00000468777.5:c.1521T=	ENSP00000419129.1:p.His507=
ENST00000469217.5:c.1488T=	ENSP00000419027.1:p.His496=
ENST00000471595.5:c.1428T=	ENSP00000417549.1:p.His476=
ENST00000473073.1:n.1629T=
ENST00000478469.5:c.885-5493T=	ENSP00000420759.1:n.885-5493T=
ENST00000482086.5:c.1080T=	ENSP00000417253.1:p.His360=
ENST00000483687.5:c.1371T=	ENSP00000420639.1:p.His457=
ENST00000484181.5:c.*109T=	ENSP00000417937.1:n.*109T=
ENST00000490504.5:c.1257T=	ENSP00000418307.1:p.His419=
NM_000532.4:c.1428T=	NP_000523.2:p.His476=
NM_001178014.1:c.1488T=	NP_001171485.1:p.His496=
NM_000532.5:c.1428T= MANE Select	NP_000523.2:p.His476=
NM_001178014.2:c.1488T=	NP_001171485.1:p.His496=