Canonical Allele Identifier: CA216854
Gene: KRT14 HGNC NCBI

Linked Data

ClinVar Variation Id: 66318
ClinVar RCV Id: RCV000056681
dbSNP Id: rs267607393
MyVariant Identifiers: chr17:g.39739526A>T (hg19) chr17:g.41583274A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583274A>T , CM000679.2:g.41583274A>T GRCh38
NC_000017.10:g.39739526A>T , CM000679.1:g.39739526A>T GRCh37
NC_000017.9:g.36993052A>T NCBI36
NG_008624.1:g.8622T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.1235T>A MANE Select ENSP00000167586.6:p.Ile412Asn
ENST00000167586.6:c.1235T>A ENSP00000167586.6:p.Ile412Asn
ENST00000441550.2:n.182T>A
ENST00000476662.1:n.685T>A
NM_000526.4:c.1235T>A NP_000517.2:p.Ile412Asn
NM_000526.5:c.1235T>A MANE Select NP_000517.3:p.Ile412Asn
Search 100 bp 5'
Search 100 bp 3'