Canonical Allele Identifier: CA2637835735
Gene: KRT14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41584051_41584052insAC , CM000679.2:g.41584051_41584052insAC GRCh38
NC_000017.10:g.39740303_39740304insAC , CM000679.1:g.39740303_39740304insAC GRCh37
NC_000017.9:g.36993829_36993830insAC NCBI36
NG_008624.1:g.7844_7845insGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.766-131_766-130insGT MANE Select ENSP00000167586.6:n.766-131_766-130insGT
ENST00000167586.6:c.766-131_766-130insGT ENSP00000167586.6:n.766-131_766-130insGT
ENST00000476662.1:n.216-131_216-130insGT
NM_000526.4:c.766-131_766-130insGT NP_000517.2:n.766-131_766-130insGT
NM_000526.5:c.766-131_766-130insGT MANE Select NP_000517.3:n.766-131_766-130insGT