Canonical Allele Identifier: CA2260085735
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41584060_41584069delinsTCTCTCTCTC , CM000679.2:g.41584060_41584069delinsTCTCTCTCTC GRCh38
NC_000017.10:g.39740312_39740321delinsTCTCTCTCTC , CM000679.1:g.39740312_39740321delinsTCTCTCTCTC GRCh37
NC_000017.9:g.36993838_36993847delinsTCTCTCTCTC NCBI36
NG_008624.1:g.7827_7836delinsGAGAGAGAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.766-148_766-139delinsGAGAGAGAGA MANE Select ENSP00000167586.6:n.766-148_766-139delinsGAGAGAGAGA
ENST00000167586.6:c.766-148_766-139delinsGAGAGAGAGA ENSP00000167586.6:n.766-148_766-139delinsGAGAGAGAGA
ENST00000476662.1:n.216-148_216-139delinsGAGAGAGAGA
NM_000526.4:c.766-148_766-139delinsGAGAGAGAGA NP_000517.2:n.766-148_766-139delinsGAGAGAGAGA
NM_000526.5:c.766-148_766-139delinsGAGAGAGAGA MANE Select NP_000517.3:n.766-148_766-139delinsGAGAGAGAGA