Canonical Allele Identifier: CA399476613
Gene: KRT14 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39739865T>A (hg19) chr17:g.41583613T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583613T>A , CM000679.2:g.41583613T>A GRCh38
NC_000017.10:g.39739865T>A , CM000679.1:g.39739865T>A GRCh37
NC_000017.9:g.36993391T>A NCBI36
NG_008624.1:g.8283A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.991A>T MANE Select ENSP00000167586.6:p.Ile331Phe
ENST00000167586.6:c.991A>T ENSP00000167586.6:p.Ile331Phe
ENST00000476662.1:n.441A>T
NM_000526.4:c.991A>T NP_000517.2:p.Ile331Phe
NM_000526.5:c.991A>T MANE Select NP_000517.3:p.Ile331Phe
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