Canonical Allele Identifier: CA83819671

Gene: PCCB

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.136326838C>G , CM000665.2:g.136326838C>G	GRCh38
NC_000003.11:g.136045680C>G , CM000665.1:g.136045680C>G	GRCh37
NC_000003.10:g.137528370C>G	NCBI36
NG_008939.1:g.81514C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000532.5:c.1126C>G MANE Select	NP_000523.2:p.Arg376Gly
ENST00000251654.9:c.1126C>G MANE Select	ENSP00000251654.4:p.Arg376Gly
NM_000532.4:c.1126C>G	NP_000523.2:p.Arg376Gly
NM_001178014.1:c.1186C>G	NP_001171485.1:p.Arg396Gly
NM_001178014.2:c.1186C>G	NP_001171485.1:p.Arg396Gly
ENST00000251654.8:c.1126C>G	ENSP00000251654.4:p.Arg376Gly
ENST00000462637.5:c.1057C>G	ENSP00000420391.1:p.Arg353Gly
ENST00000466072.5:c.1186C>G	ENSP00000420158.1:p.Arg396Gly
ENST00000468777.5:c.1219C>G	ENSP00000419129.1:p.Arg407Gly
ENST00000469217.5:c.1186C>G	ENSP00000419027.1:p.Arg396Gly
ENST00000471595.5:c.1126C>G	ENSP00000417549.1:p.Arg376Gly
ENST00000473073.1:n.1083C>G
ENST00000474833.5:n.751C>G
ENST00000475214.5:n.1040C>G
ENST00000478469.5:c.885-7442C>G	ENSP00000420759.1:n.885-7442C>G
ENST00000482086.5:c.778C>G	ENSP00000417253.1:p.Arg260Gly
ENST00000483687.5:c.1069C>G	ENSP00000420639.1:p.Arg357Gly
ENST00000484181.5:c.1126C>G	ENSP00000417937.1:p.Arg376Gly
ENST00000490504.5:c.955C>G	ENSP00000418307.1:p.Arg319Gly