Canonical Allele Identifier: CA2566641710
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41584632_41584633insATGGGCACT , CM000679.2:g.41584632_41584633insATGGGCACT GRCh38
NC_000017.10:g.39740884_39740885insATGGGCACT , CM000679.1:g.39740884_39740885insATGGGCACT GRCh37
NC_000017.9:g.36994410_36994411insATGGGCACT NCBI36
NG_008624.1:g.7263_7264insAGTGCCCAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.609-220_609-219insAGTGCCCAT MANE Select ENSP00000167586.6:n.609-220_609-219insAGTGCCCAT
ENST00000167586.6:c.609-220_609-219insAGTGCCCAT ENSP00000167586.6:n.609-220_609-219insAGTGCCCAT
NM_000526.4:c.609-220_609-219insAGTGCCCAT NP_000517.2:n.609-220_609-219insAGTGCCCAT
NM_000526.5:c.609-220_609-219insAGTGCCCAT MANE Select NP_000517.3:n.609-220_609-219insAGTGCCCAT