Canonical Allele Identifier: CA354739532

Gene: PCCB

Linked Data

• MyVariant Identifiers: chr3:g.135980804A>C (hg19) ; chr3:g.136261962A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.136261962A>C , CM000665.2:g.136261962A>C	GRCh38
NC_000003.11:g.135980804A>C , CM000665.1:g.135980804A>C	GRCh37
NC_000003.10:g.137463494A>C	NCBI36
NG_008939.1:g.16638A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251654.9:c.440A>C MANE Select	ENSP00000251654.4:p.Gln147Pro
ENST00000251654.8:c.440A>C	ENSP00000251654.4:p.Gln147Pro
ENST00000459873.1:c.191A>C	ENSP00000419293.1:p.Gln64Pro
ENST00000462542.5:c.307A>C
ENST00000462637.5:c.371A>C	ENSP00000420391.1:p.Gln124Pro
ENST00000465176.5:n.402A>C
ENST00000465423.5:c.527A>C	ENSP00000419263.1:p.Gln176Pro
ENST00000466072.5:c.440A>C	ENSP00000420158.1:p.Gln147Pro
ENST00000468777.5:c.533A>C	ENSP00000419129.1:p.Gln178Pro
ENST00000469217.5:c.500A>C	ENSP00000419027.1:p.Gln167Pro
ENST00000471595.5:c.440A>C	ENSP00000417549.1:p.Gln147Pro
ENST00000473073.1:n.397A>C
ENST00000474833.5:n.168+11404A>C
ENST00000475214.5:n.354A>C
ENST00000478469.5:c.440A>C	ENSP00000420759.1:p.Gln147Pro
ENST00000482086.5:c.94-2A>C	ENSP00000417253.1:n.94-2A>C
ENST00000483687.5:c.383A>C	ENSP00000420639.1:p.Gln128Pro
ENST00000484181.5:c.440A>C	ENSP00000417937.1:p.Gln147Pro
ENST00000490504.5:c.372+5339A>C	ENSP00000418307.1:n.372+5339A>C
ENST00000494742.5:c.191A>C	ENSP00000418020.1:p.Gln64Pro
NM_000532.4:c.440A>C	NP_000523.2:p.Gln147Pro
NM_001178014.1:c.500A>C	NP_001171485.1:p.Gln167Pro
XM_011512873.1:c.440A>C	XP_011511175.1:p.Gln147Pro
XM_011512873.2:c.440A>C	XP_011511175.1:p.Gln147Pro
NM_000532.5:c.440A>C MANE Select	NP_000523.2:p.Gln147Pro
NM_001178014.2:c.500A>C	NP_001171485.1:p.Gln167Pro