Canonical Allele Identifier: CA983758121
Gene: KRT14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41584098_41584099insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT , CM000679.2:g.41584098_41584099insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT GRCh38
NC_000017.10:g.39740350_39740351insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT , CM000679.1:g.39740350_39740351insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT GRCh37
NC_000017.9:g.36993876_36993877insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NCBI36
NG_008624.1:g.7826_7827insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.766-149_766-148insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA MANE Select ENSP00000167586.6:n.766-149_766-148insAAAAAAAAAAAAAAAAAAAAAAA...
ENST00000167586.6:c.766-149_766-148insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA ENSP00000167586.6:n.766-149_766-148insAAAAAAAAAAAAAAAAAAAAAAA...
ENST00000476662.1:n.216-149_216-148insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
NM_000526.4:c.766-149_766-148insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA NP_000517.2:n.766-149_766-148insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA...
NM_000526.5:c.766-149_766-148insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA MANE Select NP_000517.3:n.766-149_766-148insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA...