Canonical Allele Identifier: CA2101667119
Gene: KLF5 HGNC NCBI

Linked Data

dbSNP Id: rs1010552993

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.73064562del , CM000675.2:g.73064562del GRCh38
NC_000013.10:g.73638700del , CM000675.1:g.73638700del GRCh37
NC_000013.9:g.72536701del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000377687.6:c.1195+679del MANE Select ENSP00000366915.4:n.1195+679del
ENST00000377687.5:c.1195+679del ENSP00000366915.4:n.1195+679del
ENST00000539231.5:c.922+679del ENSP00000440407.1:n.922+679del
NM_001286818.1:c.922+679del NP_001273747.1:n.922+679del
NM_001730.4:c.1195+679del NP_001721.2:n.1195+679del
NM_001730.5:c.1195+679del MANE Select NP_001721.2:n.1195+679del
NM_001286818.2:c.922+679del NP_001273747.1:n.922+679del