Canonical Allele Identifier: CA2260087008
Gene: KRT14 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586742_41586743delinsGA , CM000679.2:g.41586742_41586743delinsGA GRCh38
NC_000017.10:g.39742994_39742995delinsGA , CM000679.1:g.39742994_39742995delinsGA GRCh37
NC_000017.9:g.36996520_36996521delinsGA NCBI36
NG_008624.1:g.5153_5154delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.92_93delinsTC MANE Select ENSP00000167586.6:p.Ile31=
ENST00000167586.6:c.92_93delinsTC ENSP00000167586.6:p.Ile31=
NM_000526.4:c.92_93delinsTC NP_000517.2:p.Ile31=
NM_000526.5:c.92_93delinsTC MANE Select NP_000517.3:p.Ile31=
Search 100 bp 5'
Search 100 bp 3'