Canonical Allele Identifier: CA216899
Gene: KRT14 HGNC NCBI

Linked Data

ClinVar Variation Id: 66341
dbSNP Id: rs61263401

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586480T>C , CM000679.2:g.41586480T>C GRCh38
NC_000017.10:g.39742732T>C , CM000679.1:g.39742732T>C GRCh37
NC_000017.9:g.36996258T>C NCBI36
NG_008624.1:g.5416A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.355A>G MANE Select ENSP00000167586.6:p.Met119Val
ENST00000167586.6:c.355A>G ENSP00000167586.6:p.Met119Val
NM_000526.4:c.355A>G NP_000517.2:p.Met119Val
NM_000526.5:c.355A>G MANE Select NP_000517.3:p.Met119Val