Canonical Allele Identifier: CA156191

Gene: KLF6

Linked Data

• ClinVar Variation Id: 132785
• ClinVar RCV Id: RCV000119254
• dbSNP Id: rs142749289
• ExAC: 10:3824013 G / A
• gnomAD v2: 10-3824013-G-A
• gnomAD v3: 10-3781821-G-A
• gnomAD v4: 10-3781821-G-A
• MyVariant Identifiers: chr10:g.3824013G>A (hg19) ; chr10:g.3781821G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.3781821G>A , CM000672.2:g.3781821G>A	GRCh38
NC_000010.10:g.3824013G>A , CM000672.1:g.3824013G>A	GRCh37
NC_000010.9:g.3814013G>A	NCBI36
NG_012277.1:g.8461C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000497571.6:c.496C>T MANE Select	ENSP00000419923.1:p.Pro166Ser
ENST00000173785.4:n.231C>T
ENST00000380946.3:n.731C>T
ENST00000469435.1:c.496C>T	ENSP00000419079.1:p.Pro166Ser
ENST00000497571.5:c.496C>T	ENSP00000419923.1:p.Pro166Ser
ENST00000542957.1:c.496C>T	ENSP00000445301.1:p.Pro166Ser
NM_001160124.1:c.496C>T	NP_001153596.1:p.Pro166Ser
NM_001160125.1:c.496C>T	NP_001153597.1:p.Pro166Ser
NM_001300.5:c.496C>T	NP_001291.3:p.Pro166Ser
NR_027653.1:n.763C>T
NM_001300.6:c.496C>T MANE Select	NP_001291.3:p.Pro166Ser
NM_001160124.2:c.496C>T	NP_001153596.1:p.Pro166Ser
NR_027653.2:n.691C>T
NM_001160125.2:c.496C>T	NP_001153597.1:p.Pro166Ser