Canonical Allele Identifier: CA399483092
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs11551758

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586646G>C , CM000679.2:g.41586646G>C GRCh38
NC_000017.10:g.39742898G>C , CM000679.1:g.39742898G>C GRCh37
NC_000017.9:g.36996424G>C NCBI36
NG_008624.1:g.5250C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.189C>G MANE Select ENSP00000167586.6:p.Cys63Trp
ENST00000167586.6:c.189C>G ENSP00000167586.6:p.Cys63Trp
NM_000526.4:c.189C>G NP_000517.2:p.Tyr63Ter
NM_000526.5:c.189C>G MANE Select NP_000517.3:p.Cys63Trp