Canonical Allele Identifier: CA5388762

Gene: KLF6

Linked Data

• dbSNP Id: rs754239177
• ExAC: 10:3823976 C / A
• gnomAD v2: 10-3823976-C-A
• gnomAD v4: 10-3781784-C-A
• MyVariant Identifiers: chr10:g.3823976C>A (hg19) ; chr10:g.3781784C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.3781784C>A , CM000672.2:g.3781784C>A	GRCh38
NC_000010.10:g.3823976C>A , CM000672.1:g.3823976C>A	GRCh37
NC_000010.9:g.3813976C>A	NCBI36
NG_012277.1:g.8498G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000497571.6:c.533G>T MANE Select	ENSP00000419923.1:p.Gly178Val
ENST00000173785.4:n.257+11G>T
ENST00000469435.1:c.533G>T	ENSP00000419079.1:p.Gly178Val
ENST00000497571.5:c.533G>T	ENSP00000419923.1:p.Gly178Val
ENST00000542957.1:c.533G>T	ENSP00000445301.1:p.Gly178Val
NM_001160124.1:c.533G>T	NP_001153596.1:p.Gly178Val
NM_001160125.1:c.533G>T	NP_001153597.1:p.Gly178Val
NM_001300.5:c.533G>T	NP_001291.3:p.Gly178Val
NR_027653.1:n.789+11G>T
NM_001300.6:c.533G>T MANE Select	NP_001291.3:p.Gly178Val
NM_001160124.2:c.533G>T	NP_001153596.1:p.Gly178Val
NR_027653.2:n.717+11G>T
NM_001160125.2:c.533G>T	NP_001153597.1:p.Gly178Val