Canonical Allele Identifier: CA610706598

Gene: KLF5

Linked Data

• gnomAD v2: 13-73638766-C-T
• MyVariant Identifiers: chr13:g.73638766C>T (hg19) ; chr13:g.73064628C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.73064628C>T , CM000675.2:g.73064628C>T	GRCh38
NC_000013.10:g.73638766C>T , CM000675.1:g.73638766C>T	GRCh37
NC_000013.9:g.72536767C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377687.6:c.1195+745C>T MANE Select	ENSP00000366915.4:n.1195+745C>T
ENST00000377687.5:c.1195+745C>T	ENSP00000366915.4:n.1195+745C>T
ENST00000539231.5:c.922+745C>T	ENSP00000440407.1:n.922+745C>T
NM_001286818.1:c.922+745C>T	NP_001273747.1:n.922+745C>T
NM_001730.4:c.1195+745C>T	NP_001721.2:n.1195+745C>T
NM_001730.5:c.1195+745C>T MANE Select	NP_001721.2:n.1195+745C>T
NM_001286818.2:c.922+745C>T	NP_001273747.1:n.922+745C>T