Canonical Allele Identifier: CA8562737
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs59271739
ExAC: 17:39742739 C / T
gnomAD v2: 17-39742739-C-T
COSMIC: COSM4544040
MyVariant Identifiers: chr17:g.39742739C>T (hg19) chr17:g.41586487C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586487C>T , CM000679.2:g.41586487C>T GRCh38
NC_000017.10:g.39742739C>T , CM000679.1:g.39742739C>T GRCh37
NC_000017.9:g.36996265C>T NCBI36
NG_008624.1:g.5409G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.348G>A MANE Select ENSP00000167586.6:p.Lys116=
ENST00000167586.6:c.348G>A ENSP00000167586.6:p.Lys116=
NM_000526.4:c.348G>A NP_000517.2:p.Lys116=
NM_000526.5:c.348G>A MANE Select NP_000517.3:p.Lys116=
Search 100 bp 5'
Search 100 bp 3'