Canonical Allele Identifier: CA2260087048
Gene: KRT14 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586801_41586804delinsTGGA , CM000679.2:g.41586801_41586804delinsTGGA GRCh38
NC_000017.10:g.39743053_39743056delinsTGGA , CM000679.1:g.39743053_39743056delinsTGGA GRCh37
NC_000017.9:g.36996579_36996582delinsTGGA NCBI36
NG_008624.1:g.5092_5095delinsTCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.31_34delinsTCCA MANE Select ENSP00000167586.6:p.Ser11=
ENST00000167586.6:c.31_34delinsTCCA ENSP00000167586.6:p.Ser11=
NM_000526.4:c.31_34delinsTCCA NP_000517.2:p.Ser11=
NM_000526.5:c.31_34delinsTCCA MANE Select NP_000517.3:p.Ser11=
Search 100 bp 5'
Search 100 bp 3'