Canonical Allele Identifier: CA1404305097

Gene: PCCB

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.136330058A= , CM000665.2:g.136330058A=	GRCh38
NC_000003.11:g.136048900A= , CM000665.1:g.136048900A=	GRCh37
NC_000003.10:g.137531590A=	NCBI36
NG_008939.1:g.84734A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251654.9:c.*32A= MANE Select	ENSP00000251654.4:n.*32A=
ENST00000251654.8:c.*32A=	ENSP00000251654.4:n.*32A=
ENST00000462637.5:c.*32A=	ENSP00000420391.1:n.*32A=
ENST00000466072.5:c.*32A=	ENSP00000420158.1:n.*32A=
ENST00000468777.5:c.*32A=	ENSP00000419129.1:n.*32A=
ENST00000469217.5:c.*32A=	ENSP00000419027.1:n.*32A=
ENST00000471595.5:c.1578+74A=	ENSP00000417549.1:n.1578+74A=
ENST00000473073.1:n.1853A=
ENST00000478469.5:c.885-4222A=	ENSP00000420759.1:n.885-4222A=
ENST00000482086.5:c.*32A=	ENSP00000417253.1:n.*32A=
ENST00000483687.5:c.*32A=	ENSP00000420639.1:n.*32A=
ENST00000484181.5:c.*333A=	ENSP00000417937.1:n.*333A=
ENST00000490504.5:c.*32A=	ENSP00000418307.1:n.*32A=
NM_000532.4:c.*32A=	NP_000523.2:n.*32A=
NM_001178014.1:c.*32A=	NP_001171485.1:n.*32A=
NM_000532.5:c.*32A= MANE Select	NP_000523.2:n.*32A=
NM_001178014.2:c.*32A=	NP_001171485.1:n.*32A=