Canonical Allele Identifier: CA1773202727
Gene: PNOC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.28324265_28324269delinsGGCAA , CM000670.2:g.28324265_28324269delinsGGCAA GRCh38
NC_000008.10:g.28181782_28181786delinsGGCAA , CM000670.1:g.28181782_28181786delinsGGCAA GRCh37
NC_000008.9:g.28237701_28237705delinsGGCAA NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000301908.8:c.-23-4870_-23-4866delinsGGCAA MANE Select ENSP00000301908.3:n.-23-4870_-23-4866deli...
ENST00000301908.7:c.-23-4870_-23-4866delinsGGCAA ENSP00000301908.3:n.-23-4870_-23-4866deli...
ENST00000518479.5:c.-23-4870_-23-4866delinsGGCAA ENSP00000428059.1:n.-23-4870_-23-4866deli...
NM_006228.4:c.-23-4870_-23-4866delinsGGCAA NP_006219.1:n.-23-4870_-23-4866delinsGGCA...
XM_005273532.1:c.-23-4870_-23-4866delinsGGCAA XP_005273589.1:n.-23-4870_-23-4866delinsG...
XM_011544559.1:c.-23-4870_-23-4866delinsGGCAA XP_011542861.1:n.-23-4870_-23-4866delinsG...
XM_005273532.2:c.-23-4870_-23-4866delinsGGCAA XP_005273589.1:n.-23-4870_-23-4866delinsG...
XM_011544559.2:c.-23-4870_-23-4866delinsGGCAA XP_011542861.1:n.-23-4870_-23-4866delinsG...
NM_006228.5:c.-23-4870_-23-4866delinsGGCAA MANE Select NP_006219.1:n.-23-4870_-23-4866delinsGGCA...