Canonical Allele Identifier: CA399484187
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs766646368

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586819G>T , CM000679.2:g.41586819G>T GRCh38
NC_000017.10:g.39743071G>T , CM000679.1:g.39743071G>T GRCh37
NC_000017.9:g.36996597G>T NCBI36
NG_008624.1:g.5077C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.16C>A MANE Select ENSP00000167586.6:p.Arg6Ser
ENST00000167586.6:c.16C>A ENSP00000167586.6:p.Arg6Ser
NM_000526.4:c.16C>A NP_000517.2:p.Arg6Ser
NM_000526.5:c.16C>A MANE Select NP_000517.3:p.Arg6Ser