Canonical Allele Identifier: CA399476520
Gene: KRT14 HGNC NCBI

Linked Data

COSMIC: COSM5896313
MyVariant Identifiers: chr17:g.39739846G>A (hg19) chr17:g.41583594G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583594G>A , CM000679.2:g.41583594G>A GRCh38
NC_000017.10:g.39739846G>A , CM000679.1:g.39739846G>A GRCh37
NC_000017.9:g.36993372G>A NCBI36
NG_008624.1:g.8302C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.1010C>T MANE Select ENSP00000167586.6:p.Thr337Ile
ENST00000167586.6:c.1010C>T ENSP00000167586.6:p.Thr337Ile
ENST00000476662.1:n.460C>T
NM_000526.4:c.1010C>T NP_000517.2:p.Thr337Ile
NM_000526.5:c.1010C>T MANE Select NP_000517.3:p.Thr337Ile
Search 100 bp 5'
Search 100 bp 3'