Canonical Allele Identifier: CA2101667127
Gene: KLF5 HGNC NCBI

Linked Data

dbSNP Id: rs1417928158
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.73064567T>C , CM000675.2:g.73064567T>C GRCh38
NC_000013.10:g.73638705T>C , CM000675.1:g.73638705T>C GRCh37
NC_000013.9:g.72536706T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000377687.6:c.1195+684T>C MANE Select ENSP00000366915.4:n.1195+684T>C
ENST00000377687.5:c.1195+684T>C ENSP00000366915.4:n.1195+684T>C
ENST00000539231.5:c.922+684T>C ENSP00000440407.1:n.922+684T>C
NM_001286818.1:c.922+684T>C NP_001273747.1:n.922+684T>C
NM_001730.4:c.1195+684T>C NP_001721.2:n.1195+684T>C
NM_001730.5:c.1195+684T>C MANE Select NP_001721.2:n.1195+684T>C
NM_001286818.2:c.922+684T>C NP_001273747.1:n.922+684T>C
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