Canonical Allele Identifier: CA2260087016
Gene: KRT14 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586753_41586765delinsAGCCGCCCCCGAT , CM000679.2:g.41586753_41586765delinsAGCCGCCCCCGAT GRCh38
NC_000017.10:g.39743005_39743017delinsAGCCGCCCCCGAT , CM000679.1:g.39743005_39743017delinsAGCCGCCCCCGAT GRCh37
NC_000017.9:g.36996531_36996543delinsAGCCGCCCCCGAT NCBI36
NG_008624.1:g.5131_5143delinsATCGGGGGCGGCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.70_82delinsATCGGGGGCGGCT MANE Select ENSP00000167586.6:p.Ile24=
ENST00000167586.6:c.70_82delinsATCGGGGGCGGCT ENSP00000167586.6:p.Ile24=
NM_000526.4:c.70_82delinsATCGGGGGCGGCT NP_000517.2:p.Ile24=
NM_000526.5:c.70_82delinsATCGGGGGCGGCT MANE Select NP_000517.3:p.Ile24=
Search 100 bp 5'
Search 100 bp 3'