Canonical Allele Identifier: CA8562711
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs757483555
ExAC: 17:39742616 A / ACT
gnomAD v2: 17-39742616-A-ACT
gnomAD v3: 17-41586364-A-ACT
gnomAD v4: 17-41586364-A-ACT
MyVariant Identifiers: chr17:g.39742616_39742617insCT (hg19) chr17:g.41586364_41586365insCT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586364_41586365insCT , CM000679.2:g.41586364_41586365insCT GRCh38
NC_000017.10:g.39742616_39742617insCT , CM000679.1:g.39742616_39742617insCT GRCh37
NC_000017.9:g.36996142_36996143insCT NCBI36
NG_008624.1:g.5531_5532insAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.470_471insAG MANE Select ENSP00000167586.6:p.Glu158ValfsTer16
ENST00000167586.6:c.470_471insAG ENSP00000167586.6:p.Glu158ValfsTer16
NM_000526.4:c.470_471insAG NP_000517.2:p.Glu158ValfsTer16
NM_000526.5:c.470_471insAG MANE Select NP_000517.3:p.Glu158ValfsTer16
Search 100 bp 5'
Search 100 bp 3'