Canonical Allele Identifier: CA399478193
Gene: KRT14 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39740580T>A (hg19) chr17:g.41584328T>A (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.694A>T MANE Select ENSP00000167586.6:p.Arg232Ter
ENST00000167586.6:c.694A>T ENSP00000167586.6:p.Arg232Ter
ENST00000476662.1:n.144A>T
NM_000526.4:c.694A>T NP_000517.2:p.Arg232Ter
NM_000526.5:c.694A>T MANE Select NP_000517.3:p.Arg232Ter
Search 100 bp 5'
Search 100 bp 3'