Canonical Allele Identifier: CA354645590

Gene: PCCB

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.136301028A>G , CM000665.2:g.136301028A>G	GRCh38
NC_000003.11:g.136019870A>G , CM000665.1:g.136019870A>G	GRCh37
NC_000003.10:g.137502560A>G	NCBI36
NG_008939.1:g.55704A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000532.5:c.885-2A>G MANE Select	NP_000523.2:n.885-2A>G
ENST00000251654.9:c.885-2A>G MANE Select	ENSP00000251654.4:n.885-2A>G
NM_000532.4:c.885-2A>G	NP_000523.2:n.885-2A>G
NM_001178014.1:c.945-2A>G	NP_001171485.1:n.945-2A>G
NM_001178014.2:c.945-2A>G	NP_001171485.1:n.945-2A>G
ENST00000251654.8:c.885-2A>G	ENSP00000251654.4:n.885-2A>G
ENST00000462637.5:c.816-2A>G	ENSP00000420391.1:n.816-2A>G
ENST00000466072.5:c.885-2A>G	ENSP00000420158.1:n.885-2A>G
ENST00000468777.5:c.978-2A>G	ENSP00000419129.1:n.978-2A>G
ENST00000469217.5:c.945-2A>G	ENSP00000419027.1:n.945-2A>G
ENST00000471595.5:c.885-2A>G	ENSP00000417549.1:n.885-2A>G
ENST00000473073.1:n.842-2A>G
ENST00000474833.5:n.510-2A>G
ENST00000475214.5:n.799-2A>G
ENST00000478469.5:c.884+2956A>G	ENSP00000420759.1:n.884+2956A>G
ENST00000482086.5:c.537-2A>G	ENSP00000417253.1:n.537-2A>G
ENST00000483687.5:c.828-2A>G	ENSP00000420639.1:n.828-2A>G
ENST00000484181.5:c.885-2A>G	ENSP00000417937.1:n.885-2A>G
ENST00000490504.5:c.714-2A>G	ENSP00000418307.1:n.714-2A>G
XM_011512873.1:c.885-2A>G	XP_011511175.1:n.885-2A>G
XM_011512873.2:c.885-2A>G	XP_011511175.1:n.885-2A>G