Canonical Allele Identifier: CA216863
Gene: KRT14 HGNC NCBI

Linked Data

ClinVar Variation Id: 66322
dbSNP Id: rs59442925

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583265T>C , CM000679.2:g.41583265T>C GRCh38
NC_000017.10:g.39739517T>C , CM000679.1:g.39739517T>C GRCh37
NC_000017.9:g.36993043T>C NCBI36
NG_008624.1:g.8631A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.1244A>G MANE Select ENSP00000167586.6:p.Tyr415Cys
ENST00000167586.6:c.1244A>G ENSP00000167586.6:p.Tyr415Cys
ENST00000441550.2:n.191A>G
ENST00000476662.1:n.694A>G
NM_000526.4:c.1244A>G NP_000517.2:p.Tyr415Cys
NM_000526.5:c.1244A>G MANE Select NP_000517.3:p.Tyr415Cys