Canonical Allele Identifier: CA399476286
Gene: KRT14 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39739807C>T (hg19) chr17:g.41583555C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583555C>T , CM000679.2:g.41583555C>T GRCh38
NC_000017.10:g.39739807C>T , CM000679.1:g.39739807C>T GRCh37
NC_000017.9:g.36993333C>T NCBI36
NG_008624.1:g.8341G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.1049G>A MANE Select ENSP00000167586.6:p.Ser350Asn
ENST00000167586.6:c.1049G>A ENSP00000167586.6:p.Ser350Asn
ENST00000476662.1:n.499G>A
NM_000526.4:c.1049G>A NP_000517.2:p.Ser350Asn
NM_000526.5:c.1049G>A MANE Select NP_000517.3:p.Ser350Asn
Search 100 bp 5'
Search 100 bp 3'