Canonical Allele Identifier: CA1404287810
Gene: PCCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.136261763_136261767delinsTATTA , CM000665.2:g.136261763_136261767delinsTATTA GRCh38
NC_000003.11:g.135980605_135980609delinsTATTA , CM000665.1:g.135980605_135980609delinsTATTA GRCh37
NC_000003.10:g.137463295_137463299delinsTATTA NCBI36
NG_008939.1:g.16439_16443delinsTATTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000251654.9:c.430-189_430-185delinsTATTA MANE Select ENSP00000251654.4:n.430-189_430-185delinsTATTA
ENST00000251654.8:c.430-189_430-185delinsTATTA ENSP00000251654.4:n.430-189_430-185delinsTATTA
ENST00000459873.1:c.181-189_181-185delinsTATTA ENSP00000419293.1:n.181-189_181-185delinsTATTA
ENST00000462542.5:c.297-189_297-185delinsTATTA
ENST00000462637.5:c.361-189_361-185delinsTATTA ENSP00000420391.1:n.361-189_361-185delinsTATTA
ENST00000465176.5:n.392-189_392-185delinsTATTA
ENST00000465423.5:c.517-189_517-185delinsTATTA ENSP00000419263.1:n.517-189_517-185delinsTATTA
ENST00000466072.5:c.430-189_430-185delinsTATTA ENSP00000420158.1:n.430-189_430-185delinsTATTA
ENST00000468777.5:c.523-189_523-185delinsTATTA ENSP00000419129.1:n.523-189_523-185delinsTATTA
ENST00000469217.5:c.490-189_490-185delinsTATTA ENSP00000419027.1:n.490-189_490-185delinsTATTA
ENST00000471595.5:c.430-189_430-185delinsTATTA ENSP00000417549.1:n.430-189_430-185delinsTATTA
ENST00000473073.1:n.387-189_387-185delinsTATTA
ENST00000474833.5:n.168+11205_168+11209delinsTATTA
ENST00000475214.5:n.344-189_344-185delinsTATTA
ENST00000478469.5:c.430-189_430-185delinsTATTA ENSP00000420759.1:n.430-189_430-185delinsTATTA
ENST00000482086.5:c.94-201_94-197delinsTATTA ENSP00000417253.1:n.94-201_94-197delinsTATTA
ENST00000483687.5:c.373-189_373-185delinsTATTA ENSP00000420639.1:n.373-189_373-185delinsTATTA
ENST00000484181.5:c.430-189_430-185delinsTATTA ENSP00000417937.1:n.430-189_430-185delinsTATTA
ENST00000490504.5:c.372+5140_372+5144delinsTATTA ENSP00000418307.1:n.372+5140_372+5144delinsTATTA
ENST00000494742.5:c.181-189_181-185delinsTATTA ENSP00000418020.1:n.181-189_181-185delinsTATTA
NM_000532.4:c.430-189_430-185delinsTATTA NP_000523.2:n.430-189_430-185delinsTATTA
NM_001178014.1:c.490-189_490-185delinsTATTA NP_001171485.1:n.490-189_490-185delinsTATTA
XM_011512873.1:c.430-189_430-185delinsTATTA XP_011511175.1:n.430-189_430-185delinsTATTA
XM_011512873.2:c.430-189_430-185delinsTATTA XP_011511175.1:n.430-189_430-185delinsTATTA
NM_000532.5:c.430-189_430-185delinsTATTA MANE Select NP_000523.2:n.430-189_430-185delinsTATTA
NM_001178014.2:c.490-189_490-185delinsTATTA NP_001171485.1:n.490-189_490-185delinsTATTA