Canonical Allele Identifier: CA2637835981
Gene: KRT14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41584070_41584071insCTTTTTTTTTTTTTTTT , CM000679.2:g.41584070_41584071insCTTTTTTTTTTTTTTTT GRCh38
NC_000017.10:g.39740322_39740323insCTTTTTTTTTTTTTTTT , CM000679.1:g.39740322_39740323insCTTTTTTTTTTTTTTTT GRCh37
NC_000017.9:g.36993848_36993849insCTTTTTTTTTTTTTTTT NCBI36
NG_008624.1:g.7826_7827insAAAAAAAAAAAAAAAGA

Transcript Alleles

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