Canonical Allele Identifier: CA375869606

Gene: KLF6

Linked Data

• dbSNP Id: rs1227606738
• MyVariant Identifiers: chr10:g.3824160C>G (hg19) ; chr10:g.3781968C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.3781968C>G , CM000672.2:g.3781968C>G	GRCh38
NC_000010.10:g.3824160C>G , CM000672.1:g.3824160C>G	GRCh37
NC_000010.9:g.3814160C>G	NCBI36
NG_012277.1:g.8314G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000497571.6:c.349G>C MANE Select	ENSP00000419923.1:p.Glu117Gln
ENST00000173785.4:n.84G>C
ENST00000380946.3:n.584G>C
ENST00000469435.1:c.349G>C	ENSP00000419079.1:p.Glu117Gln
ENST00000497571.5:c.349G>C	ENSP00000419923.1:p.Glu117Gln
ENST00000542957.1:c.349G>C	ENSP00000445301.1:p.Glu117Gln
NM_001160124.1:c.349G>C	NP_001153596.1:p.Glu117Gln
NM_001160125.1:c.349G>C	NP_001153597.1:p.Glu117Gln
NM_001300.5:c.349G>C	NP_001291.3:p.Glu117Gln
NR_027653.1:n.616G>C
NM_001300.6:c.349G>C MANE Select	NP_001291.3:p.Glu117Gln
NM_001160124.2:c.349G>C	NP_001153596.1:p.Glu117Gln
NR_027653.2:n.544G>C
NM_001160125.2:c.349G>C	NP_001153597.1:p.Glu117Gln