Canonical Allele Identifier: CA2260087001
Gene: KRT14 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586731_41586735delinsAGGAC , CM000679.2:g.41586731_41586735delinsAGGAC GRCh38
NC_000017.10:g.39742983_39742987delinsAGGAC , CM000679.1:g.39742983_39742987delinsAGGAC GRCh37
NC_000017.9:g.36996509_36996513delinsAGGAC NCBI36
NG_008624.1:g.5161_5165delinsGTCCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.100_104delinsGTCCT MANE Select ENSP00000167586.6:p.Val34=
ENST00000167586.6:c.100_104delinsGTCCT ENSP00000167586.6:p.Val34=
NM_000526.4:c.100_104delinsGTCCT NP_000517.2:p.Val34=
NM_000526.5:c.100_104delinsGTCCT MANE Select NP_000517.3:p.Val34=
Search 100 bp 5'
Search 100 bp 3'