Canonical Allele Identifier: CA399475236
Gene: KRT14 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39739499C>G (hg19) chr17:g.41583247C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583247C>G , CM000679.2:g.41583247C>G GRCh38
NC_000017.10:g.39739499C>G , CM000679.1:g.39739499C>G GRCh37
NC_000017.9:g.36993025C>G NCBI36
NG_008624.1:g.8649G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.1262G>C MANE Select ENSP00000167586.6:p.Gly421Ala
ENST00000167586.6:c.1262G>C ENSP00000167586.6:p.Gly421Ala
ENST00000441550.2:n.209G>C
NM_000526.4:c.1262G>C NP_000517.2:p.Gly421Ala
NM_000526.5:c.1262G>C MANE Select NP_000517.3:p.Gly421Ala
Search 100 bp 5'
Search 100 bp 3'