Canonical Allele Identifier: CA1404288006

Gene: PCCB

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.136262144_136262146delinsACT , CM000665.2:g.136262144_136262146delinsACT	GRCh38
NC_000003.11:g.135980986_135980988delinsACT , CM000665.1:g.135980986_135980988delinsACT	GRCh37
NC_000003.10:g.137463676_137463678delinsACT	NCBI36
NG_008939.1:g.16820_16822delinsACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251654.9:c.543+79_543+81delinsACT MANE Select	ENSP00000251654.4:n.543+79_543+81delinsACT
ENST00000251654.8:c.543+79_543+81delinsACT	ENSP00000251654.4:n.543+79_543+81delinsACT
ENST00000459873.1:c.294+79_294+81delinsACT	ENSP00000419293.1:n.294+79_294+81delinsACT
ENST00000462542.5:c.410+79_410+81delinsACT
ENST00000462637.5:c.474+79_474+81delinsACT	ENSP00000420391.1:n.474+79_474+81delinsACT
ENST00000465176.5:n.505+79_505+81delinsACT
ENST00000466072.5:c.543+79_543+81delinsACT	ENSP00000420158.1:n.543+79_543+81delinsACT
ENST00000468777.5:c.636+79_636+81delinsACT	ENSP00000419129.1:n.636+79_636+81delinsACT
ENST00000469217.5:c.603+79_603+81delinsACT	ENSP00000419027.1:n.603+79_603+81delinsACT
ENST00000471595.5:c.543+79_543+81delinsACT	ENSP00000417549.1:n.543+79_543+81delinsACT
ENST00000473073.1:n.500+79_500+81delinsACT
ENST00000474833.5:n.168+11586_168+11588delinsACT
ENST00000475214.5:n.457+79_457+81delinsACT
ENST00000478469.5:c.543+79_543+81delinsACT	ENSP00000420759.1:n.543+79_543+81delinsACT
ENST00000482086.5:c.195+79_195+81delinsACT	ENSP00000417253.1:n.195+79_195+81delinsACT
ENST00000483687.5:c.486+79_486+81delinsACT	ENSP00000420639.1:n.486+79_486+81delinsACT
ENST00000484181.5:c.543+79_543+81delinsACT	ENSP00000417937.1:n.543+79_543+81delinsACT
ENST00000490504.5:c.372+5521_372+5523delinsACT	ENSP00000418307.1:n.372+5521_372+5523delinsACT
NM_000532.4:c.543+79_543+81delinsACT	NP_000523.2:n.543+79_543+81delinsACT
NM_001178014.1:c.603+79_603+81delinsACT	NP_001171485.1:n.603+79_603+81delinsACT
XM_011512873.1:c.543+79_543+81delinsACT	XP_011511175.1:n.543+79_543+81delinsACT
XM_011512873.2:c.543+79_543+81delinsACT	XP_011511175.1:n.543+79_543+81delinsACT
NM_000532.5:c.543+79_543+81delinsACT MANE Select	NP_000523.2:n.543+79_543+81delinsACT
NM_001178014.2:c.603+79_603+81delinsACT	NP_001171485.1:n.603+79_603+81delinsACT