Canonical Allele Identifier: CA1404305096

Gene: PCCB

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.136330056G= , CM000665.2:g.136330056G=	GRCh38
NC_000003.11:g.136048898G= , CM000665.1:g.136048898G=	GRCh37
NC_000003.10:g.137531588G=	NCBI36
NG_008939.1:g.84732G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251654.9:c.*30G= MANE Select	ENSP00000251654.4:n.*30G=
ENST00000251654.8:c.*30G=	ENSP00000251654.4:n.*30G=
ENST00000462637.5:c.*30G=	ENSP00000420391.1:n.*30G=
ENST00000466072.5:c.*30G=	ENSP00000420158.1:n.*30G=
ENST00000468777.5:c.*30G=	ENSP00000419129.1:n.*30G=
ENST00000469217.5:c.*30G=	ENSP00000419027.1:n.*30G=
ENST00000471595.5:c.1578+72G=	ENSP00000417549.1:n.1578+72G=
ENST00000473073.1:n.1851G=
ENST00000478469.5:c.885-4224G=	ENSP00000420759.1:n.885-4224G=
ENST00000482086.5:c.*30G=	ENSP00000417253.1:n.*30G=
ENST00000483687.5:c.*30G=	ENSP00000420639.1:n.*30G=
ENST00000484181.5:c.*331G=	ENSP00000417937.1:n.*331G=
ENST00000490504.5:c.*30G=	ENSP00000418307.1:n.*30G=
NM_000532.4:c.*30G=	NP_000523.2:n.*30G=
NM_001178014.1:c.*30G=	NP_001171485.1:n.*30G=
NM_000532.5:c.*30G= MANE Select	NP_000523.2:n.*30G=
NM_001178014.2:c.*30G=	NP_001171485.1:n.*30G=