Canonical Allele Identifier: CA1404303747

Gene: PCCB

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.136327184C= , CM000665.2:g.136327184C=	GRCh38
NC_000003.11:g.136046026C= , CM000665.1:g.136046026C=	GRCh37
NC_000003.10:g.137528716C=	NCBI36
NG_008939.1:g.81860C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000532.5:c.1228C= MANE Select	NP_000523.2:p.Arg410=
ENST00000251654.9:c.1228C= MANE Select	ENSP00000251654.4:p.Arg410=
NM_000532.4:c.1228C=	NP_000523.2:p.Arg410=
NM_001178014.1:c.1288C=	NP_001171485.1:p.Arg430=
NM_001178014.2:c.1288C=	NP_001171485.1:p.Arg430=
ENST00000251654.8:c.1228C=	ENSP00000251654.4:p.Arg410=
ENST00000462637.5:c.1159C=	ENSP00000420391.1:p.Arg387=
ENST00000466072.5:c.1288C=	ENSP00000420158.1:p.Arg430=
ENST00000468777.5:c.1321C=	ENSP00000419129.1:p.Arg441=
ENST00000469217.5:c.1288C=	ENSP00000419027.1:p.Arg430=
ENST00000471595.5:c.1228C=	ENSP00000417549.1:p.Arg410=
ENST00000473073.1:n.1429C=
ENST00000474833.5:n.823+274C=
ENST00000478469.5:c.885-7096C=	ENSP00000420759.1:n.885-7096C=
ENST00000482086.5:c.880C=	ENSP00000417253.1:p.Arg294=
ENST00000483687.5:c.1171C=	ENSP00000420639.1:p.Arg391=
ENST00000484181.5:c.1198+274C=	ENSP00000417937.1:n.1198+274C=
ENST00000490504.5:c.1057C=	ENSP00000418307.1:p.Arg353=