Canonical Allele Identifier: CA1404304503

Gene: PCCB

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.136328791A= , CM000665.2:g.136328791A=	GRCh38
NC_000003.11:g.136047633A= , CM000665.1:g.136047633A=	GRCh37
NC_000003.10:g.137530323A=	NCBI36
NG_008939.1:g.83467A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000251654.9:c.1432A= MANE Select	ENSP00000251654.4:p.Asn478=
ENST00000251654.8:c.1432A=	ENSP00000251654.4:p.Asn478=
ENST00000462637.5:c.1363A=	ENSP00000420391.1:p.Asn455=
ENST00000466072.5:c.1492A=	ENSP00000420158.1:p.Asn498=
ENST00000468777.5:c.1525A=	ENSP00000419129.1:p.Asn509=
ENST00000469217.5:c.1492A=	ENSP00000419027.1:p.Asn498=
ENST00000471595.5:c.1432A=	ENSP00000417549.1:p.Asn478=
ENST00000473073.1:n.1633A=
ENST00000478469.5:c.885-5489A=	ENSP00000420759.1:n.885-5489A=
ENST00000482086.5:c.1084A=	ENSP00000417253.1:p.Asn362=
ENST00000483687.5:c.1375A=	ENSP00000420639.1:p.Asn459=
ENST00000484181.5:c.*113A=	ENSP00000417937.1:n.*113A=
ENST00000490504.5:c.1261A=	ENSP00000418307.1:p.Asn421=
NM_000532.4:c.1432A=	NP_000523.2:p.Asn478=
NM_001178014.1:c.1492A=	NP_001171485.1:p.Asn498=
NM_000532.5:c.1432A= MANE Select	NP_000523.2:p.Asn478=
NM_001178014.2:c.1492A=	NP_001171485.1:p.Asn498=