Canonical Allele Identifier: CA1404305049
Gene: PCCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.136329958G= , CM000665.2:g.136329958G= GRCh38
NC_000003.11:g.136048800G= , CM000665.1:g.136048800G= GRCh37
NC_000003.10:g.137531490G= NCBI36
NG_008939.1:g.84634G=

Transcript Alleles

HGVS Amino-acid change
ENST00000251654.9:c.1552G= MANE Select ENSP00000251654.4:p.Asp518=
ENST00000251654.8:c.1552G= ENSP00000251654.4:p.Asp518=
ENST00000462637.5:c.1483G= ENSP00000420391.1:p.Asp495=
ENST00000466072.5:c.1612G= ENSP00000420158.1:p.Asp538=
ENST00000468777.5:c.1645G= ENSP00000419129.1:p.Asp549=
ENST00000469217.5:c.1612G= ENSP00000419027.1:p.Asp538=
ENST00000471595.5:c.1552G= ENSP00000417549.1:p.Asp518=
ENST00000473073.1:n.1753G=
ENST00000478469.5:c.885-4322G= ENSP00000420759.1:n.885-4322G=
ENST00000482086.5:c.1204G= ENSP00000417253.1:p.Asp402=
ENST00000483687.5:c.1495G= ENSP00000420639.1:p.Asp499=
ENST00000484181.5:c.*233G= ENSP00000417937.1:n.*233G=
ENST00000490504.5:c.1381G= ENSP00000418307.1:p.Asp461=
NM_000532.4:c.1552G= NP_000523.2:p.Asp518=
NM_001178014.1:c.1612G= NP_001171485.1:p.Asp538=
NM_000532.5:c.1552G= MANE Select NP_000523.2:p.Asp518=
NM_001178014.2:c.1612G= NP_001171485.1:p.Asp538=