Canonical Allele Identifier: CA8562539
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs199651076
ExAC: 17:39739849 C / T
gnomAD v2: 17-39739849-C-T
gnomAD v3: 17-41583597-C-T
gnomAD v4: 17-41583597-C-T
COSMIC: COSM6457576
MyVariant Identifiers: chr17:g.39739849C>T (hg19) chr17:g.41583597C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583597C>T , CM000679.2:g.41583597C>T GRCh38
NC_000017.10:g.39739849C>T , CM000679.1:g.39739849C>T GRCh37
NC_000017.9:g.36993375C>T NCBI36
NG_008624.1:g.8299G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.1007G>A MANE Select ENSP00000167586.6:p.Arg336His
ENST00000167586.6:c.1007G>A ENSP00000167586.6:p.Arg336His
ENST00000476662.1:n.457G>A
NM_000526.4:c.1007G>A NP_000517.2:p.Arg336His
NM_000526.5:c.1007G>A MANE Select NP_000517.3:p.Arg336His
Search 100 bp 5'
Search 100 bp 3'