Canonical Allele Identifier: CA2260085320
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583275_41583278delinsTCTC , CM000679.2:g.41583275_41583278delinsTCTC GRCh38
NC_000017.10:g.39739527_39739530delinsTCTC , CM000679.1:g.39739527_39739530delinsTCTC GRCh37
NC_000017.9:g.36993053_36993056delinsTCTC NCBI36
NG_008624.1:g.8618_8621delinsGAGA

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.1231_1234delinsGAGA MANE Select ENSP00000167586.6:p.Glu411=
ENST00000167586.6:c.1231_1234delinsGAGA ENSP00000167586.6:p.Glu411=
ENST00000441550.2:n.178_181delinsGAGA
ENST00000476662.1:n.681_684delinsGAGA
NM_000526.4:c.1231_1234delinsGAGA NP_000517.2:p.Glu411=
NM_000526.5:c.1231_1234delinsGAGA MANE Select NP_000517.3:p.Glu411=