Canonical Allele Identifier: CA435841319

Gene: PCCB

Linked Data

• MyVariant Identifiers: chr3:g.136046004A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.136327162A>G , CM000665.2:g.136327162A>G	GRCh38
NC_000003.11:g.136046004A>G , CM000665.1:g.136046004A>G	GRCh37
NC_000003.10:g.137528694A>G	NCBI36
NG_008939.1:g.81838A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000251654.9:c.1206A>G MANE Select	ENSP00000251654.4:p.Ala402=
ENST00000251654.8:c.1206A>G	ENSP00000251654.4:p.Ala402=
ENST00000462637.5:c.1137A>G	ENSP00000420391.1:p.Ala379=
ENST00000466072.5:c.1266A>G	ENSP00000420158.1:p.Ala422=
ENST00000468777.5:c.1299A>G	ENSP00000419129.1:p.Ala433=
ENST00000469217.5:c.1266A>G	ENSP00000419027.1:p.Ala422=
ENST00000471595.5:c.1206A>G	ENSP00000417549.1:p.Ala402=
ENST00000473073.1:n.1407A>G
ENST00000474833.5:n.823+252A>G
ENST00000478469.5:c.885-7118A>G	ENSP00000420759.1:n.885-7118A>G
ENST00000482086.5:c.858A>G	ENSP00000417253.1:p.Ala286=
ENST00000483687.5:c.1149A>G	ENSP00000420639.1:p.Ala383=
ENST00000484181.5:c.1198+252A>G	ENSP00000417937.1:n.1198+252A>G
ENST00000490504.5:c.1035A>G	ENSP00000418307.1:p.Ala345=
NM_000532.4:c.1206A>G	NP_000523.2:p.Ala402=
NM_001178014.1:c.1266A>G	NP_001171485.1:p.Ala422=
NM_000532.5:c.1206A>G MANE Select	NP_000523.2:p.Ala402=
NM_001178014.2:c.1266A>G	NP_001171485.1:p.Ala422=