Canonical Allele Identifier: CA913102131

Gene: PCCB

Linked Data

• MyVariant Identifiers: chr3:g.135980847dup (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.136262005dup , CM000665.2:g.136262005dup	GRCh38
NC_000003.11:g.135980847dup , CM000665.1:g.135980847dup	GRCh37
NC_000003.10:g.137463537dup	NCBI36
NG_008939.1:g.16681dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251654.9:c.483dup MANE Select	ENSP00000251654.4:p.Gly162TrpfsTer?
ENST00000251654.8:c.483dup	ENSP00000251654.4:p.Gly162TrpfsTer?
ENST00000459873.1:c.234dup	ENSP00000419293.1:p.Gly79TrpfsTer?
ENST00000462542.5:c.350dup
ENST00000462637.5:c.414dup	ENSP00000420391.1:p.Gly139TrpfsTer?
ENST00000465176.5:n.445dup
ENST00000465423.5:c.570dup	ENSP00000419263.1:p.Gly191TrpfsTer?
ENST00000466072.5:c.483dup	ENSP00000420158.1:p.Gly162TrpfsTer?
ENST00000468777.5:c.576dup	ENSP00000419129.1:p.Gly193TrpfsTer?
ENST00000469217.5:c.543dup	ENSP00000419027.1:p.Gly182TrpfsTer?
ENST00000471595.5:c.483dup	ENSP00000417549.1:p.Gly162TrpfsTer?
ENST00000473073.1:n.440dup
ENST00000474833.5:n.168+11447dup
ENST00000475214.5:n.397dup
ENST00000478469.5:c.483dup	ENSP00000420759.1:p.Gly162TrpfsTer?
ENST00000482086.5:c.135dup	ENSP00000417253.1:p.Gly46TrpfsTer?
ENST00000483687.5:c.426dup	ENSP00000420639.1:p.Gly143TrpfsTer?
ENST00000484181.5:c.483dup	ENSP00000417937.1:p.Gly162TrpfsTer?
ENST00000490504.5:c.372+5382dup	ENSP00000418307.1:n.372+5382dup
ENST00000494742.5:c.234dup	ENSP00000418020.1:p.Gly79TrpfsTer?
NM_000532.4:c.483dup	NP_000523.2:p.Gly162TrpfsTer?
NM_001178014.1:c.543dup	NP_001171485.1:p.Gly182TrpfsTer?
XM_011512873.1:c.483dup	XP_011511175.1:p.Gly162TrpfsTer?
XM_011512873.2:c.483dup	XP_011511175.1:p.Gly162TrpfsTer?
NM_000532.5:c.483dup MANE Select	NP_000523.2:p.Gly162TrpfsTer?
NM_001178014.2:c.543dup	NP_001171485.1:p.Gly182TrpfsTer?