Canonical Allele Identifier: CA2260087022
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586762_41586763delinsCG , CM000679.2:g.41586762_41586763delinsCG GRCh38
NC_000017.10:g.39743014_39743015delinsCG , CM000679.1:g.39743014_39743015delinsCG GRCh37
NC_000017.9:g.36996540_36996541delinsCG NCBI36
NG_008624.1:g.5133_5134delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.72_73delinsCG MANE Select ENSP00000167586.6:p.Ile24=
ENST00000167586.6:c.72_73delinsCG ENSP00000167586.6:p.Ile24=
NM_000526.4:c.72_73delinsCG NP_000517.2:p.Ile24=
NM_000526.5:c.72_73delinsCG MANE Select NP_000517.3:p.Ile24=