Canonical Allele Identifier: CA399476630
Gene: KRT14 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39739868C>G (hg19) chr17:g.41583616C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583616C>G , CM000679.2:g.41583616C>G GRCh38
NC_000017.10:g.39739868C>G , CM000679.1:g.39739868C>G GRCh37
NC_000017.9:g.36993394C>G NCBI36
NG_008624.1:g.8280G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.988G>C MANE Select ENSP00000167586.6:p.Glu330Gln
ENST00000167586.6:c.988G>C ENSP00000167586.6:p.Glu330Gln
ENST00000476662.1:n.438G>C
NM_000526.4:c.988G>C NP_000517.2:p.Glu330Gln
NM_000526.5:c.988G>C MANE Select NP_000517.3:p.Glu330Gln
Search 100 bp 5'
Search 100 bp 3'