Canonical Allele Identifier: CA5388826

Gene: KLF6

Linked Data

• dbSNP Id: rs778831293
• ExAC: 10:3824322 G / T
• gnomAD v2: 10-3824322-G-T
• gnomAD v4: 10-3782130-G-T
• MyVariant Identifiers: chr10:g.3824322G>T (hg19) ; chr10:g.3782130G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.3782130G>T , CM000672.2:g.3782130G>T	GRCh38
NC_000010.10:g.3824322G>T , CM000672.1:g.3824322G>T	GRCh37
NC_000010.9:g.3814322G>T	NCBI36
NG_012277.1:g.8152C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000497571.6:c.187C>A MANE Select	ENSP00000419923.1:p.Leu63Met
ENST00000380946.3:n.422C>A
ENST00000469435.1:c.187C>A	ENSP00000419079.1:p.Leu63Met
ENST00000497571.5:c.187C>A	ENSP00000419923.1:p.Leu63Met
ENST00000542957.1:c.187C>A	ENSP00000445301.1:p.Leu63Met
NM_001160124.1:c.187C>A	NP_001153596.1:p.Leu63Met
NM_001160125.1:c.187C>A	NP_001153597.1:p.Leu63Met
NM_001300.5:c.187C>A	NP_001291.3:p.Leu63Met
NR_027653.1:n.454C>A
NM_001300.6:c.187C>A MANE Select	NP_001291.3:p.Leu63Met
NM_001160124.2:c.187C>A	NP_001153596.1:p.Leu63Met
NR_027653.2:n.382C>A
NM_001160125.2:c.187C>A	NP_001153597.1:p.Leu63Met