Canonical Allele Identifier: CA2101666991
Gene: KLF5 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.73064518T= , CM000675.2:g.73064518T= GRCh38
NC_000013.10:g.73638656T= , CM000675.1:g.73638656T= GRCh37
NC_000013.9:g.72536657T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000377687.6:c.1195+635T= MANE Select ENSP00000366915.4:n.1195+635T=
ENST00000377687.5:c.1195+635T= ENSP00000366915.4:n.1195+635T=
ENST00000539231.5:c.922+635T= ENSP00000440407.1:n.922+635T=
NM_001286818.1:c.922+635T= NP_001273747.1:n.922+635T=
NM_001730.4:c.1195+635T= NP_001721.2:n.1195+635T=
NM_001730.5:c.1195+635T= MANE Select NP_001721.2:n.1195+635T=
NM_001286818.2:c.922+635T= NP_001273747.1:n.922+635T=
Search 100 bp 5'
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