Canonical Allele Identifier: CA1404287942

Gene: PCCB

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.136262014A= , CM000665.2:g.136262014A=	GRCh38
NC_000003.11:g.135980856A= , CM000665.1:g.135980856A=	GRCh37
NC_000003.10:g.137463546A=	NCBI36
NG_008939.1:g.16690A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251654.9:c.492A= MANE Select	ENSP00000251654.4:p.Ala164=
ENST00000251654.8:c.492A=	ENSP00000251654.4:p.Ala164=
ENST00000459873.1:c.243A=	ENSP00000419293.1:p.Ala81=
ENST00000462542.5:c.359A=
ENST00000462637.5:c.423A=	ENSP00000420391.1:p.Ala141=
ENST00000465176.5:n.454A=
ENST00000466072.5:c.492A=	ENSP00000420158.1:p.Ala164=
ENST00000468777.5:c.585A=	ENSP00000419129.1:p.Ala195=
ENST00000469217.5:c.552A=	ENSP00000419027.1:p.Ala184=
ENST00000471595.5:c.492A=	ENSP00000417549.1:p.Ala164=
ENST00000473073.1:n.449A=
ENST00000474833.5:n.168+11456A=
ENST00000475214.5:n.406A=
ENST00000478469.5:c.492A=	ENSP00000420759.1:p.Ala164=
ENST00000482086.5:c.144A=	ENSP00000417253.1:p.Ala48=
ENST00000483687.5:c.435A=	ENSP00000420639.1:p.Ala145=
ENST00000484181.5:c.492A=	ENSP00000417937.1:p.Ala164=
ENST00000490504.5:c.372+5391A=	ENSP00000418307.1:n.372+5391A=
ENST00000494742.5:c.243A=	ENSP00000418020.1:p.Ala81=
NM_000532.4:c.492A=	NP_000523.2:p.Ala164=
NM_001178014.1:c.552A=	NP_001171485.1:p.Ala184=
XM_011512873.1:c.492A=	XP_011511175.1:p.Ala164=
XM_011512873.2:c.492A=	XP_011511175.1:p.Ala164=
NM_000532.5:c.492A= MANE Select	NP_000523.2:p.Ala164=
NM_001178014.2:c.552A=	NP_001171485.1:p.Ala184=