Canonical Allele Identifier: CA399484088
Gene: KRT14 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39743062T>G (hg19) chr17:g.41586810T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586810T>G , CM000679.2:g.41586810T>G GRCh38
NC_000017.10:g.39743062T>G , CM000679.1:g.39743062T>G GRCh37
NC_000017.9:g.36996588T>G NCBI36
NG_008624.1:g.5086A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.25A>C MANE Select ENSP00000167586.6:p.Thr9Pro
ENST00000167586.6:c.25A>C ENSP00000167586.6:p.Thr9Pro
NM_000526.4:c.25A>C NP_000517.2:p.Thr9Pro
NM_000526.5:c.25A>C MANE Select NP_000517.3:p.Thr9Pro
Search 100 bp 5'
Search 100 bp 3'