Canonical Allele Identifier: CA1404287932

Gene: PCCB

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.136261999T= , CM000665.2:g.136261999T=	GRCh38
NC_000003.11:g.135980841T= , CM000665.1:g.135980841T=	GRCh37
NC_000003.10:g.137463531T=	NCBI36
NG_008939.1:g.16675T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251654.9:c.477T= MANE Select	ENSP00000251654.4:p.Asn159=
ENST00000251654.8:c.477T=	ENSP00000251654.4:p.Asn159=
ENST00000459873.1:c.228T=	ENSP00000419293.1:p.Asn76=
ENST00000462542.5:c.344T=
ENST00000462637.5:c.408T=	ENSP00000420391.1:p.Asn136=
ENST00000465176.5:n.439T=
ENST00000465423.5:c.564T=	ENSP00000419263.1:p.Asn188=
ENST00000466072.5:c.477T=	ENSP00000420158.1:p.Asn159=
ENST00000468777.5:c.570T=	ENSP00000419129.1:p.Asn190=
ENST00000469217.5:c.537T=	ENSP00000419027.1:p.Asn179=
ENST00000471595.5:c.477T=	ENSP00000417549.1:p.Asn159=
ENST00000473073.1:n.434T=
ENST00000474833.5:n.168+11441T=
ENST00000475214.5:n.391T=
ENST00000478469.5:c.477T=	ENSP00000420759.1:p.Asn159=
ENST00000482086.5:c.129T=	ENSP00000417253.1:p.Asn43=
ENST00000483687.5:c.420T=	ENSP00000420639.1:p.Asn140=
ENST00000484181.5:c.477T=	ENSP00000417937.1:p.Asn159=
ENST00000490504.5:c.372+5376T=	ENSP00000418307.1:n.372+5376T=
ENST00000494742.5:c.228T=	ENSP00000418020.1:p.Asn76=
NM_000532.4:c.477T=	NP_000523.2:p.Asn159=
NM_001178014.1:c.537T=	NP_001171485.1:p.Asn179=
XM_011512873.1:c.477T=	XP_011511175.1:p.Asn159=
XM_011512873.2:c.477T=	XP_011511175.1:p.Asn159=
NM_000532.5:c.477T= MANE Select	NP_000523.2:p.Asn159=
NM_001178014.2:c.537T=	NP_001171485.1:p.Asn179=