Canonical Allele Identifier: CA399475787
Gene: KRT14 HGNC NCBI

Linked Data

ClinVar Variation Id: 1048024
ClinVar RCV Id: RCV001352830
dbSNP Id: rs773920224
MyVariant Identifiers: chr17:g.39739617C>A (hg19) chr17:g.41583365C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583365C>A , CM000679.2:g.41583365C>A GRCh38
NC_000017.10:g.39739617C>A , CM000679.1:g.39739617C>A GRCh37
NC_000017.9:g.36993143C>A NCBI36
NG_008624.1:g.8531G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.1144G>T MANE Select ENSP00000167586.6:p.Glu382Ter
ENST00000167586.6:c.1144G>T ENSP00000167586.6:p.Glu382Ter
ENST00000441550.2:n.91G>T
ENST00000476662.1:n.594G>T
NM_000526.4:c.1144G>T NP_000517.2:p.Glu382Ter
NM_000526.5:c.1144G>T MANE Select NP_000517.3:p.Glu382Ter
Search 100 bp 5'
Search 100 bp 3'