Canonical Allele Identifier: CA312821

Gene: PCCB

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.136293754A>G , CM000665.2:g.136293754A>G	GRCh38
NC_000003.11:g.136012596A>G , CM000665.1:g.136012596A>G	GRCh37
NC_000003.10:g.137495286A>G	NCBI36
NG_008939.1:g.48430A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000532.5:c.655-2A>G MANE Select	NP_000523.2:n.655-2A>G
ENST00000251654.9:c.655-2A>G MANE Select	ENSP00000251654.4:n.655-2A>G
NM_000532.4:c.655-2A>G	NP_000523.2:n.655-2A>G
NM_001178014.1:c.715-2A>G	NP_001171485.1:n.715-2A>G
NM_001178014.2:c.715-2A>G	NP_001171485.1:n.715-2A>G
ENST00000251654.8:c.655-2A>G	ENSP00000251654.4:n.655-2A>G
ENST00000462637.5:c.586-2A>G	ENSP00000420391.1:n.586-2A>G
ENST00000466072.5:c.655-2A>G	ENSP00000420158.1:n.655-2A>G
ENST00000468777.5:c.748-2A>G	ENSP00000419129.1:n.748-2A>G
ENST00000469217.5:c.715-2A>G	ENSP00000419027.1:n.715-2A>G
ENST00000471595.5:c.655-2A>G	ENSP00000417549.1:n.655-2A>G
ENST00000473073.1:n.612-2A>G
ENST00000474833.5:n.280-2A>G
ENST00000475214.5:n.569-2A>G
ENST00000478469.5:c.655-2A>G	ENSP00000420759.1:n.655-2A>G
ENST00000482086.5:c.307-2A>G	ENSP00000417253.1:n.307-2A>G
ENST00000483687.5:c.598-2A>G	ENSP00000420639.1:n.598-2A>G
ENST00000484181.5:c.655-2A>G	ENSP00000417937.1:n.655-2A>G
ENST00000490504.5:c.484-2A>G	ENSP00000418307.1:n.484-2A>G
XM_011512873.1:c.655-2A>G	XP_011511175.1:n.655-2A>G
XM_011512873.2:c.655-2A>G	XP_011511175.1:n.655-2A>G