Canonical Allele Identifier: CA375868259

Gene: KLF6

Linked Data

• MyVariant Identifiers: chr10:g.3823846C>G (hg19) ; chr10:g.3781654C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.3781654C>G , CM000672.2:g.3781654C>G	GRCh38
NC_000010.10:g.3823846C>G , CM000672.1:g.3823846C>G	GRCh37
NC_000010.9:g.3813846C>G	NCBI36
NG_012277.1:g.8628G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000497571.6:c.663G>C MANE Select	ENSP00000419923.1:p.Gln221His
ENST00000173785.4:n.257+141G>C
ENST00000469435.1:c.663G>C	ENSP00000419079.1:p.Gln221His
ENST00000497571.5:c.663G>C	ENSP00000419923.1:p.Gln221His
ENST00000542957.1:c.663G>C	ENSP00000445301.1:p.Gln221His
NM_001160124.1:c.550+113G>C	NP_001153596.1:n.550+113G>C
NM_001160125.1:c.663G>C	NP_001153597.1:p.Gln221His
NM_001300.5:c.663G>C	NP_001291.3:p.Gln221His
NR_027653.1:n.789+141G>C
NM_001300.6:c.663G>C MANE Select	NP_001291.3:p.Gln221His
NM_001160124.2:c.550+113G>C	NP_001153596.1:n.550+113G>C
NR_027653.2:n.717+141G>C
NM_001160125.2:c.663G>C	NP_001153597.1:p.Gln221His