Canonical Allele Identifier: CA1404303769

Gene: PCCB

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.136327239C= , CM000665.2:g.136327239C=	GRCh38
NC_000003.11:g.136046081C= , CM000665.1:g.136046081C=	GRCh37
NC_000003.10:g.137528771C=	NCBI36
NG_008939.1:g.81915C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251654.9:c.1283C= MANE Select	ENSP00000251654.4:p.Thr428=
ENST00000251654.8:c.1283C=	ENSP00000251654.4:p.Thr428=
ENST00000462637.5:c.1214C=	ENSP00000420391.1:p.Thr405=
ENST00000466072.5:c.1343C=	ENSP00000420158.1:p.Thr448=
ENST00000468777.5:c.1376C=	ENSP00000419129.1:p.Thr459=
ENST00000469217.5:c.1343C=	ENSP00000419027.1:p.Thr448=
ENST00000471595.5:c.1283C=	ENSP00000417549.1:p.Thr428=
ENST00000473073.1:n.1484C=
ENST00000474833.5:n.823+329C=
ENST00000478469.5:c.885-7041C=	ENSP00000420759.1:n.885-7041C=
ENST00000482086.5:c.935C=	ENSP00000417253.1:p.Thr312=
ENST00000483687.5:c.1226C=	ENSP00000420639.1:p.Thr409=
ENST00000484181.5:c.1198+329C=	ENSP00000417937.1:n.1198+329C=
ENST00000490504.5:c.1112C=	ENSP00000418307.1:p.Thr371=
NM_000532.4:c.1283C=	NP_000523.2:p.Thr428=
NM_001178014.1:c.1343C=	NP_001171485.1:p.Thr448=
NM_000532.5:c.1283C= MANE Select	NP_000523.2:p.Thr428=
NM_001178014.2:c.1343C=	NP_001171485.1:p.Thr448=