Canonical Allele Identifier: CA216917
Gene: KRT14 HGNC NCBI

Linked Data

ClinVar Variation Id: 66347
ClinVar RCV Id: RCV000056716
dbSNP Id: rs60399023
MyVariant Identifiers: chr17:g.39742714G>C (hg19) chr17:g.41586462G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586462G>C , CM000679.2:g.41586462G>C GRCh38
NC_000017.10:g.39742714G>C , CM000679.1:g.39742714G>C GRCh37
NC_000017.9:g.36996240G>C NCBI36
NG_008624.1:g.5434C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.373C>G MANE Select ENSP00000167586.6:p.Arg125Gly
ENST00000167586.6:c.373C>G ENSP00000167586.6:p.Arg125Gly
NM_000526.4:c.373C>G NP_000517.2:p.Arg125Gly
NM_000526.5:c.373C>G MANE Select NP_000517.3:p.Arg125Gly
Search 100 bp 5'
Search 100 bp 3'