Canonical Allele Identifier: CA1404287960

Gene: PCCB

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.136262058T= , CM000665.2:g.136262058T=	GRCh38
NC_000003.11:g.135980900T= , CM000665.1:g.135980900T=	GRCh37
NC_000003.10:g.137463590T=	NCBI36
NG_008939.1:g.16734T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251654.9:c.536T= MANE Select	ENSP00000251654.4:p.Ile179=
ENST00000251654.8:c.536T=	ENSP00000251654.4:p.Ile179=
ENST00000459873.1:c.287T=	ENSP00000419293.1:p.Ile96=
ENST00000462542.5:c.403T=
ENST00000462637.5:c.467T=	ENSP00000420391.1:p.Ile156=
ENST00000465176.5:n.498T=
ENST00000466072.5:c.536T=	ENSP00000420158.1:p.Ile179=
ENST00000468777.5:c.629T=	ENSP00000419129.1:p.Ile210=
ENST00000469217.5:c.596T=	ENSP00000419027.1:p.Ile199=
ENST00000471595.5:c.536T=	ENSP00000417549.1:p.Ile179=
ENST00000473073.1:n.493T=
ENST00000474833.5:n.168+11500T=
ENST00000475214.5:n.450T=
ENST00000478469.5:c.536T=	ENSP00000420759.1:p.Ile179=
ENST00000482086.5:c.188T=	ENSP00000417253.1:p.Ile63=
ENST00000483687.5:c.479T=	ENSP00000420639.1:p.Ile160=
ENST00000484181.5:c.536T=	ENSP00000417937.1:p.Ile179=
ENST00000490504.5:c.372+5435T=	ENSP00000418307.1:n.372+5435T=
NM_000532.4:c.536T=	NP_000523.2:p.Ile179=
NM_001178014.1:c.596T=	NP_001171485.1:p.Ile199=
XM_011512873.1:c.536T=	XP_011511175.1:p.Ile179=
XM_011512873.2:c.536T=	XP_011511175.1:p.Ile179=
NM_000532.5:c.536T= MANE Select	NP_000523.2:p.Ile179=
NM_001178014.2:c.596T=	NP_001171485.1:p.Ile199=