Canonical Allele Identifier: CA399477053
Gene: KRT14 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39740021G>C (hg19) chr17:g.41583769G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583769G>C , CM000679.2:g.41583769G>C GRCh38
NC_000017.10:g.39740021G>C , CM000679.1:g.39740021G>C GRCh37
NC_000017.9:g.36993547G>C NCBI36
NG_008624.1:g.8127C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.918C>G MANE Select ENSP00000167586.6:p.Phe306Leu
ENST00000167586.6:c.918C>G ENSP00000167586.6:p.Phe306Leu
ENST00000476662.1:n.368C>G
NM_000526.4:c.918C>G NP_000517.2:p.Phe306Leu
NM_000526.5:c.918C>G MANE Select NP_000517.3:p.Phe306Leu
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