Canonical Allele Identifier: CA2667839540
Gene: PCCB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.136262107_136262108insG , CM000665.2:g.136262107_136262108insG GRCh38
NC_000003.11:g.135980949_135980950insG , CM000665.1:g.135980949_135980950insG GRCh37
NC_000003.10:g.137463639_137463640insG NCBI36
NG_008939.1:g.16783_16784insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000251654.9:c.543+42_543+43insG MANE Select ENSP00000251654.4:n.543+42_543+43insG
ENST00000251654.8:c.543+42_543+43insG ENSP00000251654.4:n.543+42_543+43insG
ENST00000459873.1:c.294+42_294+43insG ENSP00000419293.1:n.294+42_294+43insG
ENST00000462542.5:c.410+42_410+43insG
ENST00000462637.5:c.474+42_474+43insG ENSP00000420391.1:n.474+42_474+43insG
ENST00000465176.5:n.505+42_505+43insG
ENST00000466072.5:c.543+42_543+43insG ENSP00000420158.1:n.543+42_543+43insG
ENST00000468777.5:c.636+42_636+43insG ENSP00000419129.1:n.636+42_636+43insG
ENST00000469217.5:c.603+42_603+43insG ENSP00000419027.1:n.603+42_603+43insG
ENST00000471595.5:c.543+42_543+43insG ENSP00000417549.1:n.543+42_543+43insG
ENST00000473073.1:n.500+42_500+43insG
ENST00000474833.5:n.168+11549_168+11550insG
ENST00000475214.5:n.457+42_457+43insG
ENST00000478469.5:c.543+42_543+43insG ENSP00000420759.1:n.543+42_543+43insG
ENST00000482086.5:c.195+42_195+43insG ENSP00000417253.1:n.195+42_195+43insG
ENST00000483687.5:c.486+42_486+43insG ENSP00000420639.1:n.486+42_486+43insG
ENST00000484181.5:c.543+42_543+43insG ENSP00000417937.1:n.543+42_543+43insG
ENST00000490504.5:c.372+5484_372+5485insG ENSP00000418307.1:n.372+5484_372+5485insG
NM_000532.4:c.543+42_543+43insG NP_000523.2:n.543+42_543+43insG
NM_001178014.1:c.603+42_603+43insG NP_001171485.1:n.603+42_603+43insG
XM_011512873.1:c.543+42_543+43insG XP_011511175.1:n.543+42_543+43insG
XM_011512873.2:c.543+42_543+43insG XP_011511175.1:n.543+42_543+43insG
NM_000532.5:c.543+42_543+43insG MANE Select NP_000523.2:n.543+42_543+43insG
NM_001178014.2:c.603+42_603+43insG NP_001171485.1:n.603+42_603+43insG