Canonical Allele Identifier: CA1404287945

Gene: PCCB

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.136262018A= , CM000665.2:g.136262018A=	GRCh38
NC_000003.11:g.135980860A= , CM000665.1:g.135980860A=	GRCh37
NC_000003.10:g.137463550A=	NCBI36
NG_008939.1:g.16694A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251654.9:c.496A= MANE Select	ENSP00000251654.4:p.Ile166=
ENST00000251654.8:c.496A=	ENSP00000251654.4:p.Ile166=
ENST00000459873.1:c.247A=	ENSP00000419293.1:p.Ile83=
ENST00000462542.5:c.363A=
ENST00000462637.5:c.427A=	ENSP00000420391.1:p.Ile143=
ENST00000465176.5:n.458A=
ENST00000466072.5:c.496A=	ENSP00000420158.1:p.Ile166=
ENST00000468777.5:c.589A=	ENSP00000419129.1:p.Ile197=
ENST00000469217.5:c.556A=	ENSP00000419027.1:p.Ile186=
ENST00000471595.5:c.496A=	ENSP00000417549.1:p.Ile166=
ENST00000473073.1:n.453A=
ENST00000474833.5:n.168+11460A=
ENST00000475214.5:n.410A=
ENST00000478469.5:c.496A=	ENSP00000420759.1:p.Ile166=
ENST00000482086.5:c.148A=	ENSP00000417253.1:p.Ile50=
ENST00000483687.5:c.439A=	ENSP00000420639.1:p.Ile147=
ENST00000484181.5:c.496A=	ENSP00000417937.1:p.Ile166=
ENST00000490504.5:c.372+5395A=	ENSP00000418307.1:n.372+5395A=
ENST00000494742.5:c.247A=	ENSP00000418020.1:p.Ile83=
NM_000532.4:c.496A=	NP_000523.2:p.Ile166=
NM_001178014.1:c.556A=	NP_001171485.1:p.Ile186=
XM_011512873.1:c.496A=	XP_011511175.1:p.Ile166=
XM_011512873.2:c.496A=	XP_011511175.1:p.Ile166=
NM_000532.5:c.496A= MANE Select	NP_000523.2:p.Ile166=
NM_001178014.2:c.556A=	NP_001171485.1:p.Ile186=