Canonical Allele Identifier: CA435957487

Gene: PCCB

Linked Data

• MyVariant Identifiers: chr3:g.135980880T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.136262038T>G , CM000665.2:g.136262038T>G	GRCh38
NC_000003.11:g.135980880T>G , CM000665.1:g.135980880T>G	GRCh37
NC_000003.10:g.137463570T>G	NCBI36
NG_008939.1:g.16714T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251654.9:c.516T>G MANE Select	ENSP00000251654.4:p.Ser172=
ENST00000251654.8:c.516T>G	ENSP00000251654.4:p.Ser172=
ENST00000459873.1:c.267T>G	ENSP00000419293.1:p.Ser89=
ENST00000462542.5:c.383T>G
ENST00000462637.5:c.447T>G	ENSP00000420391.1:p.Ser149=
ENST00000465176.5:n.478T>G
ENST00000466072.5:c.516T>G	ENSP00000420158.1:p.Ser172=
ENST00000468777.5:c.609T>G	ENSP00000419129.1:p.Ser203=
ENST00000469217.5:c.576T>G	ENSP00000419027.1:p.Ser192=
ENST00000471595.5:c.516T>G	ENSP00000417549.1:p.Ser172=
ENST00000473073.1:n.473T>G
ENST00000474833.5:n.168+11480T>G
ENST00000475214.5:n.430T>G
ENST00000478469.5:c.516T>G	ENSP00000420759.1:p.Ser172=
ENST00000482086.5:c.168T>G	ENSP00000417253.1:p.Ser56=
ENST00000483687.5:c.459T>G	ENSP00000420639.1:p.Ser153=
ENST00000484181.5:c.516T>G	ENSP00000417937.1:p.Ser172=
ENST00000490504.5:c.372+5415T>G	ENSP00000418307.1:n.372+5415T>G
NM_000532.4:c.516T>G	NP_000523.2:p.Ser172=
NM_001178014.1:c.576T>G	NP_001171485.1:p.Ser192=
XM_011512873.1:c.516T>G	XP_011511175.1:p.Ser172=
XM_011512873.2:c.516T>G	XP_011511175.1:p.Ser172=
NM_000532.5:c.516T>G MANE Select	NP_000523.2:p.Ser172=
NM_001178014.2:c.576T>G	NP_001171485.1:p.Ser192=