Canonical Allele Identifier: CA216925
Gene: KRT14 HGNC NCBI

Linked Data

ClinVar Variation Id: 66349
ClinVar RCV Id: RCV000056720
dbSNP Id: rs58330629

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586461C>A , CM000679.2:g.41586461C>A GRCh38
NC_000017.10:g.39742713C>A , CM000679.1:g.39742713C>A GRCh37
NC_000017.9:g.36996239C>A NCBI36
NG_008624.1:g.5435G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.374G>T MANE Select ENSP00000167586.6:p.Arg125Leu
ENST00000167586.6:c.374G>T ENSP00000167586.6:p.Arg125Leu
NM_000526.4:c.374G>T NP_000517.2:p.Arg125Leu
NM_000526.5:c.374G>T MANE Select NP_000517.3:p.Arg125Leu