Canonical Allele Identifier: CA2260085743
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41584066_41584069delinsTCTC , CM000679.2:g.41584066_41584069delinsTCTC GRCh38
NC_000017.10:g.39740318_39740321delinsTCTC , CM000679.1:g.39740318_39740321delinsTCTC GRCh37
NC_000017.9:g.36993844_36993847delinsTCTC NCBI36
NG_008624.1:g.7827_7830delinsGAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.766-148_766-145delinsGAGA MANE Select ENSP00000167586.6:n.766-148_766-145delinsGAGA
ENST00000167586.6:c.766-148_766-145delinsGAGA ENSP00000167586.6:n.766-148_766-145delinsGAGA
ENST00000476662.1:n.216-148_216-145delinsGAGA
NM_000526.4:c.766-148_766-145delinsGAGA NP_000517.2:n.766-148_766-145delinsGAGA
NM_000526.5:c.766-148_766-145delinsGAGA MANE Select NP_000517.3:n.766-148_766-145delinsGAGA