Canonical Allele Identifier: CA1404305046

Gene: PCCB

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.136329948A= , CM000665.2:g.136329948A=	GRCh38
NC_000003.11:g.136048790A= , CM000665.1:g.136048790A=	GRCh37
NC_000003.10:g.137531480A=	NCBI36
NG_008939.1:g.84624A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000251654.9:c.1542A= MANE Select	ENSP00000251654.4:p.Arg514=
ENST00000251654.8:c.1542A=	ENSP00000251654.4:p.Arg514=
ENST00000462637.5:c.1473A=	ENSP00000420391.1:p.Arg491=
ENST00000466072.5:c.1602A=	ENSP00000420158.1:p.Arg534=
ENST00000468777.5:c.1635A=	ENSP00000419129.1:p.Arg545=
ENST00000469217.5:c.1602A=	ENSP00000419027.1:p.Arg534=
ENST00000471595.5:c.1542A=	ENSP00000417549.1:p.Arg514=
ENST00000473073.1:n.1743A=
ENST00000478469.5:c.885-4332A=	ENSP00000420759.1:n.885-4332A=
ENST00000482086.5:c.1194A=	ENSP00000417253.1:p.Arg398=
ENST00000483687.5:c.1485A=	ENSP00000420639.1:p.Arg495=
ENST00000484181.5:c.*223A=	ENSP00000417937.1:n.*223A=
ENST00000490504.5:c.1371A=	ENSP00000418307.1:p.Arg457=
NM_000532.4:c.1542A=	NP_000523.2:p.Arg514=
NM_001178014.1:c.1602A=	NP_001171485.1:p.Arg534=
NM_000532.5:c.1542A= MANE Select	NP_000523.2:p.Arg514=
NM_001178014.2:c.1602A=	NP_001171485.1:p.Arg534=