Canonical Allele Identifier: CA2101666954
Gene: KLF5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.73064509T= , CM000675.2:g.73064509T= GRCh38
NC_000013.10:g.73638647T= , CM000675.1:g.73638647T= GRCh37
NC_000013.9:g.72536648T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000377687.6:c.1195+626T= MANE Select ENSP00000366915.4:n.1195+626T=
ENST00000377687.5:c.1195+626T= ENSP00000366915.4:n.1195+626T=
ENST00000539231.5:c.922+626T= ENSP00000440407.1:n.922+626T=
NM_001286818.1:c.922+626T= NP_001273747.1:n.922+626T=
NM_001730.4:c.1195+626T= NP_001721.2:n.1195+626T=
NM_001730.5:c.1195+626T= MANE Select NP_001721.2:n.1195+626T=
NM_001286818.2:c.922+626T= NP_001273747.1:n.922+626T=