Canonical Allele Identifier: CA1404303728

Gene: PCCB

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.136327163C= , CM000665.2:g.136327163C=	GRCh38
NC_000003.11:g.136046005C= , CM000665.1:g.136046005C=	GRCh37
NC_000003.10:g.137528695C=	NCBI36
NG_008939.1:g.81839C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000251654.9:c.1207C= MANE Select	ENSP00000251654.4:p.Gln403=
ENST00000251654.8:c.1207C=	ENSP00000251654.4:p.Gln403=
ENST00000462637.5:c.1138C=	ENSP00000420391.1:p.Gln380=
ENST00000466072.5:c.1267C=	ENSP00000420158.1:p.Gln423=
ENST00000468777.5:c.1300C=	ENSP00000419129.1:p.Gln434=
ENST00000469217.5:c.1267C=	ENSP00000419027.1:p.Gln423=
ENST00000471595.5:c.1207C=	ENSP00000417549.1:p.Gln403=
ENST00000473073.1:n.1408C=
ENST00000474833.5:n.823+253C=
ENST00000478469.5:c.885-7117C=	ENSP00000420759.1:n.885-7117C=
ENST00000482086.5:c.859C=	ENSP00000417253.1:p.Gln287=
ENST00000483687.5:c.1150C=	ENSP00000420639.1:p.Gln384=
ENST00000484181.5:c.1198+253C=	ENSP00000417937.1:n.1198+253C=
ENST00000490504.5:c.1036C=	ENSP00000418307.1:p.Gln346=
NM_000532.4:c.1207C=	NP_000523.2:p.Gln403=
NM_001178014.1:c.1267C=	NP_001171485.1:p.Gln423=
NM_000532.5:c.1207C= MANE Select	NP_000523.2:p.Gln403=
NM_001178014.2:c.1267C=	NP_001171485.1:p.Gln423=