Canonical Allele Identifier: CA2608059600

Gene: KLF6

Linked Data

• gnomAD v4: 10-3781608-CGGCCGCCCTCCGG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.3781613_3781625del , CM000672.2:g.3781613_3781625del	GRCh38
NC_000010.10:g.3823805_3823817del , CM000672.1:g.3823805_3823817del	GRCh37
NC_000010.9:g.3813805_3813817del	NCBI36
NG_012277.1:g.8661_8673del

Transcript Alleles

HGVS	Amino-acid change
ENST00000497571.6:c.676+20_676+32del MANE Select	ENSP00000419923.1:n.676+20_676+32del
ENST00000173785.4:n.257+174_257+186del
ENST00000469435.1:c.696_708del	ENSP00000419079.1:p.Arg233LeufsTer?
ENST00000497571.5:c.676+20_676+32del	ENSP00000419923.1:n.676+20_676+32del
ENST00000542957.1:c.676+20_676+32del	ENSP00000445301.1:n.676+20_676+32del
NM_001160124.1:c.550+146_550+158del	NP_001153596.1:n.550+146_550+158del
NM_001160125.1:c.676+20_676+32del	NP_001153597.1:n.676+20_676+32del
NM_001300.5:c.676+20_676+32del	NP_001291.3:n.676+20_676+32del
NR_027653.1:n.789+174_789+186del
NM_001300.6:c.676+20_676+32del MANE Select	NP_001291.3:n.676+20_676+32del
NM_001160124.2:c.550+146_550+158del	NP_001153596.1:n.550+146_550+158del
NR_027653.2:n.717+174_717+186del
NM_001160125.2:c.676+20_676+32del	NP_001153597.1:n.676+20_676+32del