Canonical Allele Identifier: CA1404287953

Gene: PCCB

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.136262042G= , CM000665.2:g.136262042G=	GRCh38
NC_000003.11:g.135980884G= , CM000665.1:g.135980884G=	GRCh37
NC_000003.10:g.137463574G=	NCBI36
NG_008939.1:g.16718G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251654.9:c.520G= MANE Select	ENSP00000251654.4:p.Ala174=
ENST00000251654.8:c.520G=	ENSP00000251654.4:p.Ala174=
ENST00000459873.1:c.271G=	ENSP00000419293.1:p.Ala91=
ENST00000462542.5:c.387G=
ENST00000462637.5:c.451G=	ENSP00000420391.1:p.Ala151=
ENST00000465176.5:n.482G=
ENST00000466072.5:c.520G=	ENSP00000420158.1:p.Ala174=
ENST00000468777.5:c.613G=	ENSP00000419129.1:p.Ala205=
ENST00000469217.5:c.580G=	ENSP00000419027.1:p.Ala194=
ENST00000471595.5:c.520G=	ENSP00000417549.1:p.Ala174=
ENST00000473073.1:n.477G=
ENST00000474833.5:n.168+11484G=
ENST00000475214.5:n.434G=
ENST00000478469.5:c.520G=	ENSP00000420759.1:p.Ala174=
ENST00000482086.5:c.172G=	ENSP00000417253.1:p.Ala58=
ENST00000483687.5:c.463G=	ENSP00000420639.1:p.Ala155=
ENST00000484181.5:c.520G=	ENSP00000417937.1:p.Ala174=
ENST00000490504.5:c.372+5419G=	ENSP00000418307.1:n.372+5419G=
NM_000532.4:c.520G=	NP_000523.2:p.Ala174=
NM_001178014.1:c.580G=	NP_001171485.1:p.Ala194=
XM_011512873.1:c.520G=	XP_011511175.1:p.Ala174=
XM_011512873.2:c.520G=	XP_011511175.1:p.Ala174=
NM_000532.5:c.520G= MANE Select	NP_000523.2:p.Ala174=
NM_001178014.2:c.580G=	NP_001171485.1:p.Ala194=