Canonical Allele Identifier: CA399477057
Gene: KRT14 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39740022A>G (hg19) chr17:g.41583770A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583770A>G , CM000679.2:g.41583770A>G GRCh38
NC_000017.10:g.39740022A>G , CM000679.1:g.39740022A>G GRCh37
NC_000017.9:g.36993548A>G NCBI36
NG_008624.1:g.8126T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.917T>C MANE Select ENSP00000167586.6:p.Phe306Ser
ENST00000167586.6:c.917T>C ENSP00000167586.6:p.Phe306Ser
ENST00000476662.1:n.367T>C
NM_000526.4:c.917T>C NP_000517.2:p.Phe306Ser
NM_000526.5:c.917T>C MANE Select NP_000517.3:p.Phe306Ser
Search 100 bp 5'
Search 100 bp 3'