Canonical Allele Identifier: CA1404287839

Gene: PCCB

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.136261811G= , CM000665.2:g.136261811G=	GRCh38
NC_000003.11:g.135980653G= , CM000665.1:g.135980653G=	GRCh37
NC_000003.10:g.137463343G=	NCBI36
NG_008939.1:g.16487G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000251654.9:c.430-141G= MANE Select	ENSP00000251654.4:n.430-141G=
ENST00000251654.8:c.430-141G=	ENSP00000251654.4:n.430-141G=
ENST00000459873.1:c.181-141G=	ENSP00000419293.1:n.181-141G=
ENST00000462542.5:c.297-141G=
ENST00000462637.5:c.361-141G=	ENSP00000420391.1:n.361-141G=
ENST00000465176.5:n.392-141G=
ENST00000465423.5:c.517-141G=	ENSP00000419263.1:n.517-141G=
ENST00000466072.5:c.430-141G=	ENSP00000420158.1:n.430-141G=
ENST00000468777.5:c.523-141G=	ENSP00000419129.1:n.523-141G=
ENST00000469217.5:c.490-141G=	ENSP00000419027.1:n.490-141G=
ENST00000471595.5:c.430-141G=	ENSP00000417549.1:n.430-141G=
ENST00000473073.1:n.387-141G=
ENST00000474833.5:n.168+11253G=
ENST00000475214.5:n.344-141G=
ENST00000478469.5:c.430-141G=	ENSP00000420759.1:n.430-141G=
ENST00000482086.5:c.94-153G=	ENSP00000417253.1:n.94-153G=
ENST00000483687.5:c.373-141G=	ENSP00000420639.1:n.373-141G=
ENST00000484181.5:c.430-141G=	ENSP00000417937.1:n.430-141G=
ENST00000490504.5:c.372+5188G=	ENSP00000418307.1:n.372+5188G=
ENST00000494742.5:c.181-141G=	ENSP00000418020.1:n.181-141G=
NM_000532.4:c.430-141G=	NP_000523.2:n.430-141G=
NM_001178014.1:c.490-141G=	NP_001171485.1:n.490-141G=
XM_011512873.1:c.430-141G=	XP_011511175.1:n.430-141G=
XM_011512873.2:c.430-141G=	XP_011511175.1:n.430-141G=
NM_000532.5:c.430-141G= MANE Select	NP_000523.2:n.430-141G=
NM_001178014.2:c.490-141G=	NP_001171485.1:n.490-141G=