Canonical Allele Identifier: CA252600094
Gene: KLF5 HGNC NCBI

Linked Data

dbSNP Id: rs988504132
gnomAD v3: 13-73064548-G-A
gnomAD v4: 13-73064548-G-A
MyVariant Identifiers: chr13:g.73638686G>A (hg19) chr13:g.73064548G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.73064548G>A , CM000675.2:g.73064548G>A GRCh38
NC_000013.10:g.73638686G>A , CM000675.1:g.73638686G>A GRCh37
NC_000013.9:g.72536687G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000377687.6:c.1195+665G>A MANE Select ENSP00000366915.4:n.1195+665G>A
ENST00000377687.5:c.1195+665G>A ENSP00000366915.4:n.1195+665G>A
ENST00000539231.5:c.922+665G>A ENSP00000440407.1:n.922+665G>A
NM_001286818.1:c.922+665G>A NP_001273747.1:n.922+665G>A
NM_001730.4:c.1195+665G>A NP_001721.2:n.1195+665G>A
NM_001730.5:c.1195+665G>A MANE Select NP_001721.2:n.1195+665G>A
NM_001286818.2:c.922+665G>A NP_001273747.1:n.922+665G>A
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