Canonical Allele Identifier: CA290665171
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs921071074
MyVariant Identifiers: chr17:g.39740666C>T (hg19) chr17:g.41584414C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41584414C>T , CM000679.2:g.41584414C>T GRCh38
NC_000017.10:g.39740666C>T , CM000679.1:g.39740666C>T GRCh37
NC_000017.9:g.36994192C>T NCBI36
NG_008624.1:g.7482G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.609-1G>A MANE Select ENSP00000167586.6:n.609-1G>A
ENST00000167586.6:c.609-1G>A ENSP00000167586.6:n.609-1G>A
ENST00000476662.1:n.58G>A
NM_000526.4:c.609-1G>A NP_000517.2:n.609-1G>A
NM_000526.5:c.609-1G>A MANE Select NP_000517.3:n.609-1G>A
Search 100 bp 5'
Search 100 bp 3'