Canonical Allele Identifier: CA1404287957

Gene: PCCB

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.136262048T= , CM000665.2:g.136262048T=	GRCh38
NC_000003.11:g.135980890T= , CM000665.1:g.135980890T=	GRCh37
NC_000003.10:g.137463580T=	NCBI36
NG_008939.1:g.16724T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251654.9:c.526T= MANE Select	ENSP00000251654.4:p.Tyr176=
ENST00000251654.8:c.526T=	ENSP00000251654.4:p.Tyr176=
ENST00000459873.1:c.277T=	ENSP00000419293.1:p.Tyr93=
ENST00000462542.5:c.393T=
ENST00000462637.5:c.457T=	ENSP00000420391.1:p.Tyr153=
ENST00000465176.5:n.488T=
ENST00000466072.5:c.526T=	ENSP00000420158.1:p.Tyr176=
ENST00000468777.5:c.619T=	ENSP00000419129.1:p.Tyr207=
ENST00000469217.5:c.586T=	ENSP00000419027.1:p.Tyr196=
ENST00000471595.5:c.526T=	ENSP00000417549.1:p.Tyr176=
ENST00000473073.1:n.483T=
ENST00000474833.5:n.168+11490T=
ENST00000475214.5:n.440T=
ENST00000478469.5:c.526T=	ENSP00000420759.1:p.Tyr176=
ENST00000482086.5:c.178T=	ENSP00000417253.1:p.Tyr60=
ENST00000483687.5:c.469T=	ENSP00000420639.1:p.Tyr157=
ENST00000484181.5:c.526T=	ENSP00000417937.1:p.Tyr176=
ENST00000490504.5:c.372+5425T=	ENSP00000418307.1:n.372+5425T=
NM_000532.4:c.526T=	NP_000523.2:p.Tyr176=
NM_001178014.1:c.586T=	NP_001171485.1:p.Tyr196=
XM_011512873.1:c.526T=	XP_011511175.1:p.Tyr176=
XM_011512873.2:c.526T=	XP_011511175.1:p.Tyr176=
NM_000532.5:c.526T= MANE Select	NP_000523.2:p.Tyr176=
NM_001178014.2:c.586T=	NP_001171485.1:p.Tyr196=