Canonical Allele Identifier: CA1404305066

Gene: PCCB

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.136329994C= , CM000665.2:g.136329994C=	GRCh38
NC_000003.11:g.136048836C= , CM000665.1:g.136048836C=	GRCh37
NC_000003.10:g.137531526C=	NCBI36
NG_008939.1:g.84670C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251654.9:c.1588C= MANE Select	ENSP00000251654.4:p.Pro530=
ENST00000251654.8:c.1588C=	ENSP00000251654.4:p.Pro530=
ENST00000462637.5:c.1519C=	ENSP00000420391.1:p.Pro507=
ENST00000466072.5:c.1648C=	ENSP00000420158.1:p.Pro550=
ENST00000468777.5:c.1681C=	ENSP00000419129.1:p.Pro561=
ENST00000469217.5:c.1648C=	ENSP00000419027.1:p.Pro550=
ENST00000471595.5:c.1578+10C=	ENSP00000417549.1:n.1578+10C=
ENST00000473073.1:n.1789C=
ENST00000478469.5:c.885-4286C=	ENSP00000420759.1:n.885-4286C=
ENST00000482086.5:c.1240C=	ENSP00000417253.1:p.Pro414=
ENST00000483687.5:c.1531C=	ENSP00000420639.1:p.Pro511=
ENST00000484181.5:c.*269C=	ENSP00000417937.1:n.*269C=
ENST00000490504.5:c.1417C=	ENSP00000418307.1:p.Pro473=
NM_000532.4:c.1588C=	NP_000523.2:p.Pro530=
NM_001178014.1:c.1648C=	NP_001171485.1:p.Pro550=
NM_000532.5:c.1588C= MANE Select	NP_000523.2:p.Pro530=
NM_001178014.2:c.1648C=	NP_001171485.1:p.Pro550=