Canonical Allele Identifier: CA500205705
Gene: KRT14 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39740144A>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583892A>C , CM000679.2:g.41583892A>C GRCh38
NC_000017.10:g.39740144A>C , CM000679.1:g.39740144A>C GRCh37
NC_000017.9:g.36993670A>C NCBI36
NG_008624.1:g.8004T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.795T>G MANE Select ENSP00000167586.6:p.Gly265=
ENST00000167586.6:c.795T>G ENSP00000167586.6:p.Gly265=
ENST00000476662.1:n.245T>G
NM_000526.4:c.795T>G NP_000517.2:p.Gly265=
NM_000526.5:c.795T>G MANE Select NP_000517.3:p.Gly265=
Search 100 bp 5'
Search 100 bp 3'