Canonical Allele Identifier: CA983757992
Gene: KRT14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41584055_41584076del , CM000679.2:g.41584055_41584076del GRCh38
NC_000017.10:g.39740307_39740328del , CM000679.1:g.39740307_39740328del GRCh37
NC_000017.9:g.36993833_36993854del NCBI36
NG_008624.1:g.7821_7842del

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.766-154_766-133del MANE Select ENSP00000167586.6:n.766-154_766-133del
ENST00000167586.6:c.766-154_766-133del ENSP00000167586.6:n.766-154_766-133del
ENST00000476662.1:n.216-154_216-133del
NM_000526.4:c.766-154_766-133del NP_000517.2:n.766-154_766-133del
NM_000526.5:c.766-154_766-133del MANE Select NP_000517.3:n.766-154_766-133del