Canonical Allele Identifier: CA468166553

Gene: KLF6

Linked Data

• dbSNP Id: rs772132474
• gnomAD v2: 10-3823908-G-T
• MyVariant Identifiers: chr10:g.3823908G>T (hg19) ; chr10:g.3781716G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.3781716G>T , CM000672.2:g.3781716G>T	GRCh38
NC_000010.10:g.3823908G>T , CM000672.1:g.3823908G>T	GRCh37
NC_000010.9:g.3813908G>T	NCBI36
NG_012277.1:g.8566C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000497571.6:c.601C>A MANE Select	ENSP00000419923.1:p.Arg201=
ENST00000173785.4:n.257+79C>A
ENST00000469435.1:c.601C>A	ENSP00000419079.1:p.Arg201=
ENST00000497571.5:c.601C>A	ENSP00000419923.1:p.Arg201=
ENST00000542957.1:c.601C>A	ENSP00000445301.1:p.Arg201=
NM_001160124.1:c.550+51C>A	NP_001153596.1:n.550+51C>A
NM_001160125.1:c.601C>A	NP_001153597.1:p.Arg201=
NM_001300.5:c.601C>A	NP_001291.3:p.Arg201=
NR_027653.1:n.789+79C>A
NM_001300.6:c.601C>A MANE Select	NP_001291.3:p.Arg201=
NM_001160124.2:c.550+51C>A	NP_001153596.1:n.550+51C>A
NR_027653.2:n.717+79C>A
NM_001160125.2:c.601C>A	NP_001153597.1:p.Arg201=