Canonical Allele Identifier: CA2809495499
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586762dup , CM000679.2:g.41586762dup GRCh38
NC_000017.10:g.39743014dup , CM000679.1:g.39743014dup GRCh37
NC_000017.9:g.36996540dup NCBI36
NG_008624.1:g.5138dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.77dup MANE Select ENSP00000167586.6:p.Gly27ArgfsTer?
ENST00000167586.6:c.77dup ENSP00000167586.6:p.Gly27ArgfsTer?
NM_000526.4:c.77dup NP_000517.2:p.Gly27ArgfsTer?
NM_000526.5:c.77dup MANE Select NP_000517.3:p.Gly27ArgfsTer?