Canonical Allele Identifier: CA916084092

Gene: PCCB

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.136260525_136261952dup , CM000665.2:g.136260525_136261952dup	GRCh38
NC_000003.11:g.135979367_135980794dup , CM000665.1:g.135979367_135980794dup	GRCh37
NC_000003.10:g.137462057_137463484dup	NCBI36
NG_008939.1:g.15201_16628dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251654.9:c.419_430dup
ENST00000251654.8:c.419_430dup
ENST00000459873.1:c.170_181dup
ENST00000462542.5:c.286_297dup
ENST00000462637.5:c.350_361dup
ENST00000465176.5:n.381_392dup
ENST00000465423.5:c.506_517dup
ENST00000466072.5:c.419_430dup
ENST00000468777.5:c.512_523dup
ENST00000469217.5:c.479_490dup
ENST00000471595.5:c.419_430dup
ENST00000473073.1:n.376_387dup
ENST00000474833.5:n.168+9967_168+11394dup
ENST00000475214.5:n.333_344dup
ENST00000478469.5:c.419_430dup
ENST00000482086.5:c.94-1439_94-12dup	ENSP00000417253.1:n.94-1439_94-12dup
ENST00000483687.5:c.373-1427_373dup
ENST00000484181.5:c.419_430dup
ENST00000490504.5:c.372+3902_372+5329dup	ENSP00000418307.1:n.372+3902_372+5329dup
ENST00000494742.5:c.170_181dup
NM_000532.4:c.419_430dup
NM_001178014.1:c.479_490dup
XM_011512873.1:c.419_430dup
XM_011512873.2:c.419_430dup
NM_000532.5:c.419_430dup
NM_001178014.2:c.479_490dup