Canonical Allele Identifier: CA399478389
Gene: KRT14 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39740612A>C (hg19) chr17:g.41584360A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41584360A>C , CM000679.2:g.41584360A>C GRCh38
NC_000017.10:g.39740612A>C , CM000679.1:g.39740612A>C GRCh37
NC_000017.9:g.36994138A>C NCBI36
NG_008624.1:g.7536T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.662T>G MANE Select ENSP00000167586.6:p.Leu221Arg
ENST00000167586.6:c.662T>G ENSP00000167586.6:p.Leu221Arg
ENST00000476662.1:n.112T>G
NM_000526.4:c.662T>G NP_000517.2:p.Leu221Arg
NM_000526.5:c.662T>G MANE Select NP_000517.3:p.Leu221Arg
Search 100 bp 5'
Search 100 bp 3'