Canonical Allele Identifier: CA354739976

Gene: PCCB

Linked Data

• MyVariant Identifiers: chr3:g.135980893G>C (hg19) ; chr3:g.136262051G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.136262051G>C , CM000665.2:g.136262051G>C	GRCh38
NC_000003.11:g.135980893G>C , CM000665.1:g.135980893G>C	GRCh37
NC_000003.10:g.137463583G>C	NCBI36
NG_008939.1:g.16727G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251654.9:c.529G>C MANE Select	ENSP00000251654.4:p.Ala177Pro
ENST00000251654.8:c.529G>C	ENSP00000251654.4:p.Ala177Pro
ENST00000459873.1:c.280G>C	ENSP00000419293.1:p.Ala94Pro
ENST00000462542.5:c.396G>C
ENST00000462637.5:c.460G>C	ENSP00000420391.1:p.Ala154Pro
ENST00000465176.5:n.491G>C
ENST00000466072.5:c.529G>C	ENSP00000420158.1:p.Ala177Pro
ENST00000468777.5:c.622G>C	ENSP00000419129.1:p.Ala208Pro
ENST00000469217.5:c.589G>C	ENSP00000419027.1:p.Ala197Pro
ENST00000471595.5:c.529G>C	ENSP00000417549.1:p.Ala177Pro
ENST00000473073.1:n.486G>C
ENST00000474833.5:n.168+11493G>C
ENST00000475214.5:n.443G>C
ENST00000478469.5:c.529G>C	ENSP00000420759.1:p.Ala177Pro
ENST00000482086.5:c.181G>C	ENSP00000417253.1:p.Ala61Pro
ENST00000483687.5:c.472G>C	ENSP00000420639.1:p.Ala158Pro
ENST00000484181.5:c.529G>C	ENSP00000417937.1:p.Ala177Pro
ENST00000490504.5:c.372+5428G>C	ENSP00000418307.1:n.372+5428G>C
NM_000532.4:c.529G>C	NP_000523.2:p.Ala177Pro
NM_001178014.1:c.589G>C	NP_001171485.1:p.Ala197Pro
XM_011512873.1:c.529G>C	XP_011511175.1:p.Ala177Pro
XM_011512873.2:c.529G>C	XP_011511175.1:p.Ala177Pro
NM_000532.5:c.529G>C MANE Select	NP_000523.2:p.Ala177Pro
NM_001178014.2:c.589G>C	NP_001171485.1:p.Ala197Pro