Canonical Allele Identifier: CA626215435
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs1267928901
gnomAD v2: 17-39743023-CCCCGATGCCGCA-C
gnomAD v3: 17-41586771-CCCCGATGCCGCA-C
gnomAD v4: 17-41586771-CCCCGATGCCGCA-C
MyVariant Identifiers: chr17:g.39743024_39743035del (hg19) chr17:g.41586772_41586783del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586772_41586783del , CM000679.2:g.41586772_41586783del GRCh38
NC_000017.10:g.39743024_39743035del , CM000679.1:g.39743024_39743035del GRCh37
NC_000017.9:g.36996550_36996561del NCBI36
NG_008624.1:g.5113_5124del

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.52_63del MANE Select ENSP00000167586.6:p.Cys18_Gly21del
ENST00000167586.6:c.52_63del ENSP00000167586.6:p.Cys18_Gly21del
NM_000526.4:c.52_63del NP_000517.2:p.Cys18_Gly21del
NM_000526.5:c.52_63del MANE Select NP_000517.3:p.Cys18_Gly21del
Search 100 bp 5'
Search 100 bp 3'