Canonical Allele Identifier: CA399483684
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs1597800161
MyVariant Identifiers: chr17:g.39743017T>A (hg19) chr17:g.41586765T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586765T>A , CM000679.2:g.41586765T>A GRCh38
NC_000017.10:g.39743017T>A , CM000679.1:g.39743017T>A GRCh37
NC_000017.9:g.36996543T>A NCBI36
NG_008624.1:g.5131A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.70A>T MANE Select ENSP00000167586.6:p.Ile24Phe
ENST00000167586.6:c.70A>T ENSP00000167586.6:p.Ile24Phe
NM_000526.4:c.70A>T NP_000517.2:p.Ile24Phe
NM_000526.5:c.70A>T MANE Select NP_000517.3:p.Ile24Phe
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