Canonical Allele Identifier: CA626215460
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs1162202958
gnomAD v2: 17-39743104-TGAGC-T
gnomAD v3: 17-41586852-TGAGC-T
gnomAD v4: 17-41586852-TGAGC-T
MyVariant Identifiers: chr17:g.39743105_39743108del (hg19) chr17:g.41586853_41586856del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586861_41586864del , CM000679.2:g.41586861_41586864del GRCh38
NC_000017.10:g.39743113_39743116del , CM000679.1:g.39743113_39743116del GRCh37
NC_000017.9:g.36996639_36996642del NCBI36
NG_008624.1:g.5040_5043del

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.-22_-19del MANE Select ENSP00000167586.6:n.-22_-19del
ENST00000167586.6:c.-22_-19del ENSP00000167586.6:n.-22_-19del
NM_000526.4:c.-22_-19del NP_000517.2:n.-22_-19del
NM_000526.5:c.-22_-19del MANE Select NP_000517.3:n.-22_-19del
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