Canonical Allele Identifier: CA399481877
Gene: KRT14 HGNC NCBI

Linked Data

gnomAD v4: 17-41586347-C-T
MyVariant Identifiers: chr17:g.39742599C>T (hg19) chr17:g.41586347C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586347C>T , CM000679.2:g.41586347C>T GRCh38
NC_000017.10:g.39742599C>T , CM000679.1:g.39742599C>T GRCh37
NC_000017.9:g.36996125C>T NCBI36
NG_008624.1:g.5549G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.488G>A MANE Select ENSP00000167586.6:p.Ser163Asn
ENST00000167586.6:c.488G>A ENSP00000167586.6:p.Ser163Asn
NM_000526.4:c.488G>A NP_000517.2:p.Ser163Asn
NM_000526.5:c.488G>A MANE Select NP_000517.3:p.Ser163Asn
Search 100 bp 5'
Search 100 bp 3'