Canonical Allele Identifier: CA354739549

Gene: PCCB

Linked Data

• gnomAD v4: 3-136261965-C-T
• MyVariant Identifiers: chr3:g.135980807C>T (hg19) ; chr3:g.136261965C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.136261965C>T , CM000665.2:g.136261965C>T	GRCh38
NC_000003.11:g.135980807C>T , CM000665.1:g.135980807C>T	GRCh37
NC_000003.10:g.137463497C>T	NCBI36
NG_008939.1:g.16641C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251654.9:c.443C>T MANE Select	ENSP00000251654.4:p.Ala148Val
ENST00000251654.8:c.443C>T	ENSP00000251654.4:p.Ala148Val
ENST00000459873.1:c.194C>T	ENSP00000419293.1:p.Ala65Val
ENST00000462542.5:c.310C>T
ENST00000462637.5:c.374C>T	ENSP00000420391.1:p.Ala125Val
ENST00000465176.5:n.405C>T
ENST00000465423.5:c.530C>T	ENSP00000419263.1:p.Ala177Val
ENST00000466072.5:c.443C>T	ENSP00000420158.1:p.Ala148Val
ENST00000468777.5:c.536C>T	ENSP00000419129.1:p.Ala179Val
ENST00000469217.5:c.503C>T	ENSP00000419027.1:p.Ala168Val
ENST00000471595.5:c.443C>T	ENSP00000417549.1:p.Ala148Val
ENST00000473073.1:n.400C>T
ENST00000474833.5:n.168+11407C>T
ENST00000475214.5:n.357C>T
ENST00000478469.5:c.443C>T	ENSP00000420759.1:p.Ala148Val
ENST00000482086.5:c.95C>T	ENSP00000417253.1:p.Ala32Val
ENST00000483687.5:c.386C>T	ENSP00000420639.1:p.Ala129Val
ENST00000484181.5:c.443C>T	ENSP00000417937.1:p.Ala148Val
ENST00000490504.5:c.372+5342C>T	ENSP00000418307.1:n.372+5342C>T
ENST00000494742.5:c.194C>T	ENSP00000418020.1:p.Ala65Val
NM_000532.4:c.443C>T	NP_000523.2:p.Ala148Val
NM_001178014.1:c.503C>T	NP_001171485.1:p.Ala168Val
XM_011512873.1:c.443C>T	XP_011511175.1:p.Ala148Val
XM_011512873.2:c.443C>T	XP_011511175.1:p.Ala148Val
NM_000532.5:c.443C>T MANE Select	NP_000523.2:p.Ala148Val
NM_001178014.2:c.503C>T	NP_001171485.1:p.Ala168Val