Canonical Allele Identifier: CA252600101

Gene: KLF5

Linked Data

• dbSNP Id: rs532932378
• gnomAD v2: 13-73638729-TGTAGTGCA-T
• gnomAD v3: 13-73064591-TGTAGTGCA-T
• gnomAD v4: 13-73064591-TGTAGTGCA-T
• MyVariant Identifiers: chr13:g.73638730_73638737del (hg19) ; chr13:g.73064592_73064599del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.73064594_73064601del , CM000675.2:g.73064594_73064601del	GRCh38
NC_000013.10:g.73638732_73638739del , CM000675.1:g.73638732_73638739del	GRCh37
NC_000013.9:g.72536733_72536740del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377687.6:c.1195+711_1195+718del MANE Select	ENSP00000366915.4:n.1195+711_1195+718del
ENST00000377687.5:c.1195+711_1195+718del	ENSP00000366915.4:n.1195+711_1195+718del
ENST00000539231.5:c.922+711_922+718del	ENSP00000440407.1:n.922+711_922+718del
NM_001286818.1:c.922+711_922+718del	NP_001273747.1:n.922+711_922+718del
NM_001730.4:c.1195+711_1195+718del	NP_001721.2:n.1195+711_1195+718del
NM_001730.5:c.1195+711_1195+718del MANE Select	NP_001721.2:n.1195+711_1195+718del
NM_001286818.2:c.922+711_922+718del	NP_001273747.1:n.922+711_922+718del