Canonical Allele Identifier: CA1404287925
Gene: PCCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.136261982C= , CM000665.2:g.136261982C= GRCh38
NC_000003.11:g.135980824C= , CM000665.1:g.135980824C= GRCh37
NC_000003.10:g.137463514C= NCBI36
NG_008939.1:g.16658C=

Transcript Alleles

HGVS Amino-acid change
ENST00000251654.9:c.460C= MANE Select ENSP00000251654.4:p.Pro154=
ENST00000251654.8:c.460C= ENSP00000251654.4:p.Pro154=
ENST00000459873.1:c.211C= ENSP00000419293.1:p.Pro71=
ENST00000462542.5:c.327C=
ENST00000462637.5:c.391C= ENSP00000420391.1:p.Pro131=
ENST00000465176.5:n.422C=
ENST00000465423.5:c.547C= ENSP00000419263.1:p.Pro183=
ENST00000466072.5:c.460C= ENSP00000420158.1:p.Pro154=
ENST00000468777.5:c.553C= ENSP00000419129.1:p.Pro185=
ENST00000469217.5:c.520C= ENSP00000419027.1:p.Pro174=
ENST00000471595.5:c.460C= ENSP00000417549.1:p.Pro154=
ENST00000473073.1:n.417C=
ENST00000474833.5:n.168+11424C=
ENST00000475214.5:n.374C=
ENST00000478469.5:c.460C= ENSP00000420759.1:p.Pro154=
ENST00000482086.5:c.112C= ENSP00000417253.1:p.Pro38=
ENST00000483687.5:c.403C= ENSP00000420639.1:p.Pro135=
ENST00000484181.5:c.460C= ENSP00000417937.1:p.Pro154=
ENST00000490504.5:c.372+5359C= ENSP00000418307.1:n.372+5359C=
ENST00000494742.5:c.211C= ENSP00000418020.1:p.Pro71=
NM_000532.4:c.460C= NP_000523.2:p.Pro154=
NM_001178014.1:c.520C= NP_001171485.1:p.Pro174=
XM_011512873.1:c.460C= XP_011511175.1:p.Pro154=
XM_011512873.2:c.460C= XP_011511175.1:p.Pro154=
NM_000532.5:c.460C= MANE Select NP_000523.2:p.Pro154=
NM_001178014.2:c.520C= NP_001171485.1:p.Pro174=