Canonical Allele Identifier: CA399483676
Gene: KRT14 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39743016A>C (hg19) chr17:g.41586764A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586764A>C , CM000679.2:g.41586764A>C GRCh38
NC_000017.10:g.39743016A>C , CM000679.1:g.39743016A>C GRCh37
NC_000017.9:g.36996542A>C NCBI36
NG_008624.1:g.5132T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.71T>G MANE Select ENSP00000167586.6:p.Ile24Ser
ENST00000167586.6:c.71T>G ENSP00000167586.6:p.Ile24Ser
NM_000526.4:c.71T>G NP_000517.2:p.Ile24Ser
NM_000526.5:c.71T>G MANE Select NP_000517.3:p.Ile24Ser
Search 100 bp 5'
Search 100 bp 3'