Canonical Allele Identifier: CA1404287933

Gene: PCCB

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.136262002C= , CM000665.2:g.136262002C=	GRCh38
NC_000003.11:g.135980844C= , CM000665.1:g.135980844C=	GRCh37
NC_000003.10:g.137463534C=	NCBI36
NG_008939.1:g.16678C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251654.9:c.480C= MANE Select	ENSP00000251654.4:p.Asp160=
ENST00000251654.8:c.480C=	ENSP00000251654.4:p.Asp160=
ENST00000459873.1:c.231C=	ENSP00000419293.1:p.Asp77=
ENST00000462542.5:c.347C=
ENST00000462637.5:c.411C=	ENSP00000420391.1:p.Asp137=
ENST00000465176.5:n.442C=
ENST00000465423.5:c.567C=	ENSP00000419263.1:p.Asp189=
ENST00000466072.5:c.480C=	ENSP00000420158.1:p.Asp160=
ENST00000468777.5:c.573C=	ENSP00000419129.1:p.Asp191=
ENST00000469217.5:c.540C=	ENSP00000419027.1:p.Asp180=
ENST00000471595.5:c.480C=	ENSP00000417549.1:p.Asp160=
ENST00000473073.1:n.437C=
ENST00000474833.5:n.168+11444C=
ENST00000475214.5:n.394C=
ENST00000478469.5:c.480C=	ENSP00000420759.1:p.Asp160=
ENST00000482086.5:c.132C=	ENSP00000417253.1:p.Asp44=
ENST00000483687.5:c.423C=	ENSP00000420639.1:p.Asp141=
ENST00000484181.5:c.480C=	ENSP00000417937.1:p.Asp160=
ENST00000490504.5:c.372+5379C=	ENSP00000418307.1:n.372+5379C=
ENST00000494742.5:c.231C=	ENSP00000418020.1:p.Asp77=
NM_000532.4:c.480C=	NP_000523.2:p.Asp160=
NM_001178014.1:c.540C=	NP_001171485.1:p.Asp180=
XM_011512873.1:c.480C=	XP_011511175.1:p.Asp160=
XM_011512873.2:c.480C=	XP_011511175.1:p.Asp160=
NM_000532.5:c.480C= MANE Select	NP_000523.2:p.Asp160=
NM_001178014.2:c.540C=	NP_001171485.1:p.Asp180=