Canonical Allele Identifier: CA626215531
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs1162984156
gnomAD v2: 17-39740285-T-TTC
gnomAD v3: 17-41584033-T-TTC
gnomAD v4: 17-41584033-T-TTC
MyVariant Identifiers: chr17:g.39740302_39740309delinsTCAATCTCTC (hg19) chr17:g.39740285_39740286insTC (hg19) chr17:g.41584050_41584057delinsTCAATCTCTC (hg38) chr17:g.41584033_41584034insTC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41584048_41584049dup , CM000679.2:g.41584048_41584049dup GRCh38
NC_000017.10:g.39740300_39740301dup , CM000679.1:g.39740300_39740301dup GRCh37
NC_000017.9:g.36993826_36993827dup NCBI36
NG_008624.1:g.7861_7862dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.766-114_766-113dup MANE Select ENSP00000167586.6:n.766-114_766-113dup
ENST00000167586.6:c.766-114_766-113dup ENSP00000167586.6:n.766-114_766-113dup
ENST00000476662.1:n.216-114_216-113dup
NM_000526.4:c.766-114_766-113dup NP_000517.2:n.766-114_766-113dup
NM_000526.5:c.766-114_766-113dup MANE Select NP_000517.3:n.766-114_766-113dup
Search 100 bp 5'
Search 100 bp 3'