Canonical Allele Identifier: CA2637837926
Gene: KRT14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586855_41586857del , CM000679.2:g.41586855_41586857del GRCh38
NC_000017.10:g.39743107_39743109del , CM000679.1:g.39743107_39743109del GRCh37
NC_000017.9:g.36996633_36996635del NCBI36
NG_008624.1:g.5039_5041del

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.-23_-21del MANE Select ENSP00000167586.6:n.-23_-21del
ENST00000167586.6:c.-23_-21del ENSP00000167586.6:n.-23_-21del
NM_000526.4:c.-23_-21del NP_000517.2:n.-23_-21del
NM_000526.5:c.-23_-21del MANE Select NP_000517.3:n.-23_-21del