Canonical Allele Identifier: CA399477323
Gene: KRT14 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39740067T>A (hg19) chr17:g.41583815T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583815T>A , CM000679.2:g.41583815T>A GRCh38
NC_000017.10:g.39740067T>A , CM000679.1:g.39740067T>A GRCh37
NC_000017.9:g.36993593T>A NCBI36
NG_008624.1:g.8081A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.872A>T MANE Select ENSP00000167586.6:p.Tyr291Phe
ENST00000167586.6:c.872A>T ENSP00000167586.6:p.Tyr291Phe
ENST00000476662.1:n.322A>T
NM_000526.4:c.872A>T NP_000517.2:p.Tyr291Phe
NM_000526.5:c.872A>T MANE Select NP_000517.3:p.Tyr291Phe
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