Canonical Allele Identifier: CA2260086964
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586677_41586681delinsGAGAC , CM000679.2:g.41586677_41586681delinsGAGAC GRCh38
NC_000017.10:g.39742929_39742933delinsGAGAC , CM000679.1:g.39742929_39742933delinsGAGAC GRCh37
NC_000017.9:g.36996455_36996459delinsGAGAC NCBI36
NG_008624.1:g.5215_5219delinsGTCTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.154_158delinsGTCTC MANE Select ENSP00000167586.6:p.Val52=
ENST00000167586.6:c.154_158delinsGTCTC ENSP00000167586.6:p.Val52=
NM_000526.4:c.154_158delinsGTCTC NP_000517.2:p.Val52=
NM_000526.5:c.154_158delinsGTCTC MANE Select NP_000517.3:p.Val52=