Canonical Allele Identifier: CA375868660

Gene: KLF6

Linked Data

• dbSNP Id: rs2131098246
• gnomAD v3: 10-3781769-G-A
• gnomAD v4: 10-3781769-G-A
• MyVariant Identifiers: chr10:g.3823961G>A (hg19) ; chr10:g.3781769G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.3781769G>A , CM000672.2:g.3781769G>A	GRCh38
NC_000010.10:g.3823961G>A , CM000672.1:g.3823961G>A	GRCh37
NC_000010.9:g.3813961G>A	NCBI36
NG_012277.1:g.8513C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000497571.6:c.548C>T MANE Select	ENSP00000419923.1:p.Pro183Leu
ENST00000173785.4:n.257+26C>T
ENST00000469435.1:c.548C>T	ENSP00000419079.1:p.Pro183Leu
ENST00000497571.5:c.548C>T	ENSP00000419923.1:p.Pro183Leu
ENST00000542957.1:c.548C>T	ENSP00000445301.1:p.Pro183Leu
NM_001160124.1:c.548C>T	NP_001153596.1:p.Pro183Leu
NM_001160125.1:c.548C>T	NP_001153597.1:p.Pro183Leu
NM_001300.5:c.548C>T	NP_001291.3:p.Pro183Leu
NR_027653.1:n.789+26C>T
NM_001300.6:c.548C>T MANE Select	NP_001291.3:p.Pro183Leu
NM_001160124.2:c.548C>T	NP_001153596.1:p.Pro183Leu
NR_027653.2:n.717+26C>T
NM_001160125.2:c.548C>T	NP_001153597.1:p.Pro183Leu