Canonical Allele Identifier: CA1404305008
Gene: PCCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.136329874A= , CM000665.2:g.136329874A= GRCh38
NC_000003.11:g.136048716A= , CM000665.1:g.136048716A= GRCh37
NC_000003.10:g.137531406A= NCBI36
NG_008939.1:g.84550A=

Transcript Alleles

HGVS Amino-acid change
ENST00000251654.9:c.1499-31A= MANE Select ENSP00000251654.4:n.1499-31A=
ENST00000251654.8:c.1499-31A= ENSP00000251654.4:n.1499-31A=
ENST00000462637.5:c.1430-31A= ENSP00000420391.1:n.1430-31A=
ENST00000466072.5:c.1559-31A= ENSP00000420158.1:n.1559-31A=
ENST00000468777.5:c.1592-31A= ENSP00000419129.1:n.1592-31A=
ENST00000469217.5:c.1559-31A= ENSP00000419027.1:n.1559-31A=
ENST00000471595.5:c.1499-31A= ENSP00000417549.1:n.1499-31A=
ENST00000473073.1:n.1700-31A=
ENST00000478469.5:c.885-4406A= ENSP00000420759.1:n.885-4406A=
ENST00000482086.5:c.1151-31A= ENSP00000417253.1:n.1151-31A=
ENST00000483687.5:c.1442-31A= ENSP00000420639.1:n.1442-31A=
ENST00000484181.5:c.*180-31A= ENSP00000417937.1:n.*180-31A=
ENST00000490504.5:c.1328-31A= ENSP00000418307.1:n.1328-31A=
NM_000532.4:c.1499-31A= NP_000523.2:n.1499-31A=
NM_001178014.1:c.1559-31A= NP_001171485.1:n.1559-31A=
NM_000532.5:c.1499-31A= MANE Select NP_000523.2:n.1499-31A=
NM_001178014.2:c.1559-31A= NP_001171485.1:n.1559-31A=