Canonical Allele Identifier: CA2260087020
Gene: KRT14 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586757_41586758delinsGC , CM000679.2:g.41586757_41586758delinsGC GRCh38
NC_000017.10:g.39743009_39743010delinsGC , CM000679.1:g.39743009_39743010delinsGC GRCh37
NC_000017.9:g.36996535_36996536delinsGC NCBI36
NG_008624.1:g.5138_5139delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.77_78delinsGC MANE Select ENSP00000167586.6:p.Gly26=
ENST00000167586.6:c.77_78delinsGC ENSP00000167586.6:p.Gly26=
NM_000526.4:c.77_78delinsGC NP_000517.2:p.Gly26=
NM_000526.5:c.77_78delinsGC MANE Select NP_000517.3:p.Gly26=
Search 100 bp 5'
Search 100 bp 3'