Canonical Allele Identifier: CA499989782
Gene: KRT14 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39740580T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41584328T>G , CM000679.2:g.41584328T>G GRCh38
NC_000017.10:g.39740580T>G , CM000679.1:g.39740580T>G GRCh37
NC_000017.9:g.36994106T>G NCBI36
NG_008624.1:g.7568A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.694A>C MANE Select ENSP00000167586.6:p.Arg232=
ENST00000167586.6:c.694A>C ENSP00000167586.6:p.Arg232=
ENST00000476662.1:n.144A>C
NM_000526.4:c.694A>C NP_000517.2:p.Arg232=
NM_000526.5:c.694A>C MANE Select NP_000517.3:p.Arg232=
Search 100 bp 5'
Search 100 bp 3'