Canonical Allele Identifier: CA1404305047

Gene: PCCB

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.136329953G= , CM000665.2:g.136329953G=	GRCh38
NC_000003.11:g.136048795G= , CM000665.1:g.136048795G=	GRCh37
NC_000003.10:g.137531485G=	NCBI36
NG_008939.1:g.84629G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000251654.9:c.1547G= MANE Select	ENSP00000251654.4:p.Cys516=
ENST00000251654.8:c.1547G=	ENSP00000251654.4:p.Cys516=
ENST00000462637.5:c.1478G=	ENSP00000420391.1:p.Cys493=
ENST00000466072.5:c.1607G=	ENSP00000420158.1:p.Cys536=
ENST00000468777.5:c.1640G=	ENSP00000419129.1:p.Cys547=
ENST00000469217.5:c.1607G=	ENSP00000419027.1:p.Cys536=
ENST00000471595.5:c.1547G=	ENSP00000417549.1:p.Cys516=
ENST00000473073.1:n.1748G=
ENST00000478469.5:c.885-4327G=	ENSP00000420759.1:n.885-4327G=
ENST00000482086.5:c.1199G=	ENSP00000417253.1:p.Cys400=
ENST00000483687.5:c.1490G=	ENSP00000420639.1:p.Cys497=
ENST00000484181.5:c.*228G=	ENSP00000417937.1:n.*228G=
ENST00000490504.5:c.1376G=	ENSP00000418307.1:p.Cys459=
NM_000532.4:c.1547G=	NP_000523.2:p.Cys516=
NM_001178014.1:c.1607G=	NP_001171485.1:p.Cys536=
NM_000532.5:c.1547G= MANE Select	NP_000523.2:p.Cys516=
NM_001178014.2:c.1607G=	NP_001171485.1:p.Cys536=