Canonical Allele Identifier: CA1404287938

Gene: PCCB

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.136262007G= , CM000665.2:g.136262007G=	GRCh38
NC_000003.11:g.135980849G= , CM000665.1:g.135980849G=	GRCh37
NC_000003.10:g.137463539G=	NCBI36
NG_008939.1:g.16683G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251654.9:c.485G= MANE Select	ENSP00000251654.4:p.Gly162=
ENST00000251654.8:c.485G=	ENSP00000251654.4:p.Gly162=
ENST00000459873.1:c.236G=	ENSP00000419293.1:p.Gly79=
ENST00000462542.5:c.352G=
ENST00000462637.5:c.416G=	ENSP00000420391.1:p.Gly139=
ENST00000465176.5:n.447G=
ENST00000465423.5:c.572G=	ENSP00000419263.1:p.Gly191=
ENST00000466072.5:c.485G=	ENSP00000420158.1:p.Gly162=
ENST00000468777.5:c.578G=	ENSP00000419129.1:p.Gly193=
ENST00000469217.5:c.545G=	ENSP00000419027.1:p.Gly182=
ENST00000471595.5:c.485G=	ENSP00000417549.1:p.Gly162=
ENST00000473073.1:n.442G=
ENST00000474833.5:n.168+11449G=
ENST00000475214.5:n.399G=
ENST00000478469.5:c.485G=	ENSP00000420759.1:p.Gly162=
ENST00000482086.5:c.137G=	ENSP00000417253.1:p.Gly46=
ENST00000483687.5:c.428G=	ENSP00000420639.1:p.Gly143=
ENST00000484181.5:c.485G=	ENSP00000417937.1:p.Gly162=
ENST00000490504.5:c.372+5384G=	ENSP00000418307.1:n.372+5384G=
ENST00000494742.5:c.236G=	ENSP00000418020.1:p.Gly79=
NM_000532.4:c.485G=	NP_000523.2:p.Gly162=
NM_001178014.1:c.545G=	NP_001171485.1:p.Gly182=
XM_011512873.1:c.485G=	XP_011511175.1:p.Gly162=
XM_011512873.2:c.485G=	XP_011511175.1:p.Gly162=
NM_000532.5:c.485G= MANE Select	NP_000523.2:p.Gly162=
NM_001178014.2:c.545G=	NP_001171485.1:p.Gly182=