Canonical Allele Identifier: CA1404304496

Gene: PCCB

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.136328783G= , CM000665.2:g.136328783G=	GRCh38
NC_000003.11:g.136047625G= , CM000665.1:g.136047625G=	GRCh37
NC_000003.10:g.137530315G=	NCBI36
NG_008939.1:g.83459G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000251654.9:c.1424G= MANE Select	ENSP00000251654.4:p.Gly475=
ENST00000251654.8:c.1424G=	ENSP00000251654.4:p.Gly475=
ENST00000462637.5:c.1355G=	ENSP00000420391.1:p.Gly452=
ENST00000466072.5:c.1484G=	ENSP00000420158.1:p.Gly495=
ENST00000468777.5:c.1517G=	ENSP00000419129.1:p.Gly506=
ENST00000469217.5:c.1484G=	ENSP00000419027.1:p.Gly495=
ENST00000471595.5:c.1424G=	ENSP00000417549.1:p.Gly475=
ENST00000473073.1:n.1625G=
ENST00000478469.5:c.885-5497G=	ENSP00000420759.1:n.885-5497G=
ENST00000482086.5:c.1076G=	ENSP00000417253.1:p.Gly359=
ENST00000483687.5:c.1367G=	ENSP00000420639.1:p.Gly456=
ENST00000484181.5:c.*105G=	ENSP00000417937.1:n.*105G=
ENST00000490504.5:c.1253G=	ENSP00000418307.1:p.Gly418=
NM_000532.4:c.1424G=	NP_000523.2:p.Gly475=
NM_001178014.1:c.1484G=	NP_001171485.1:p.Gly495=
NM_000532.5:c.1424G= MANE Select	NP_000523.2:p.Gly475=
NM_001178014.2:c.1484G=	NP_001171485.1:p.Gly495=