Canonical Allele Identifier: CA354739634

Gene: PCCB

Linked Data

• MyVariant Identifiers: chr3:g.135980840A>C (hg19) ; chr3:g.136261998A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.136261998A>C , CM000665.2:g.136261998A>C	GRCh38
NC_000003.11:g.135980840A>C , CM000665.1:g.135980840A>C	GRCh37
NC_000003.10:g.137463530A>C	NCBI36
NG_008939.1:g.16674A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251654.9:c.476A>C MANE Select	ENSP00000251654.4:p.Asn159Thr
ENST00000251654.8:c.476A>C	ENSP00000251654.4:p.Asn159Thr
ENST00000459873.1:c.227A>C	ENSP00000419293.1:p.Asn76Thr
ENST00000462542.5:c.343A>C
ENST00000462637.5:c.407A>C	ENSP00000420391.1:p.Asn136Thr
ENST00000465176.5:n.438A>C
ENST00000465423.5:c.563A>C	ENSP00000419263.1:p.Asn188Thr
ENST00000466072.5:c.476A>C	ENSP00000420158.1:p.Asn159Thr
ENST00000468777.5:c.569A>C	ENSP00000419129.1:p.Asn190Thr
ENST00000469217.5:c.536A>C	ENSP00000419027.1:p.Asn179Thr
ENST00000471595.5:c.476A>C	ENSP00000417549.1:p.Asn159Thr
ENST00000473073.1:n.433A>C
ENST00000474833.5:n.168+11440A>C
ENST00000475214.5:n.390A>C
ENST00000478469.5:c.476A>C	ENSP00000420759.1:p.Asn159Thr
ENST00000482086.5:c.128A>C	ENSP00000417253.1:p.Asn43Thr
ENST00000483687.5:c.419A>C	ENSP00000420639.1:p.Asn140Thr
ENST00000484181.5:c.476A>C	ENSP00000417937.1:p.Asn159Thr
ENST00000490504.5:c.372+5375A>C	ENSP00000418307.1:n.372+5375A>C
ENST00000494742.5:c.227A>C	ENSP00000418020.1:p.Asn76Thr
NM_000532.4:c.476A>C	NP_000523.2:p.Asn159Thr
NM_001178014.1:c.536A>C	NP_001171485.1:p.Asn179Thr
XM_011512873.1:c.476A>C	XP_011511175.1:p.Asn159Thr
XM_011512873.2:c.476A>C	XP_011511175.1:p.Asn159Thr
NM_000532.5:c.476A>C MANE Select	NP_000523.2:p.Asn159Thr
NM_001178014.2:c.536A>C	NP_001171485.1:p.Asn179Thr