Canonical Allele Identifier: CA2260085936
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs1907458498

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41584423_41584424insATTGGCATTGT , CM000679.2:g.41584423_41584424insATTGGCATTGT GRCh38
NC_000017.10:g.39740675_39740676insATTGGCATTGT , CM000679.1:g.39740675_39740676insATTGGCATTGT GRCh37
NC_000017.9:g.36994201_36994202insATTGGCATTGT NCBI36
NG_008624.1:g.7472_7473insACAATGCCAAT

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.609-11_609-10insACAATGCCAAT MANE Select ENSP00000167586.6:n.609-11_609-10insACAAT...
ENST00000167586.6:c.609-11_609-10insACAATGCCAAT ENSP00000167586.6:n.609-11_609-10insACAAT...
ENST00000476662.1:n.48_49insACAATGCCAAT
NM_000526.4:c.609-11_609-10insACAATGCCAAT NP_000517.2:n.609-11_609-10insACAATGCCAAT...
NM_000526.5:c.609-11_609-10insACAATGCCAAT MANE Select NP_000517.3:n.609-11_609-10insACAATGCCAAT...