Canonical Allele Identifier: CA375867944

Gene: KLF6

Linked Data

• MyVariant Identifiers: chr10:g.3823784C>G (hg19) ; chr10:g.3781592C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.3781592C>G , CM000672.2:g.3781592C>G	GRCh38
NC_000010.10:g.3823784C>G , CM000672.1:g.3823784C>G	GRCh37
NC_000010.9:g.3813784C>G	NCBI36
NG_012277.1:g.8690G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000497571.6:c.676+49G>C MANE Select	ENSP00000419923.1:n.676+49G>C
ENST00000173785.4:n.257+203G>C
ENST00000469435.1:c.725G>C	ENSP00000419079.1:p.Cys242Ser
ENST00000497571.5:c.676+49G>C	ENSP00000419923.1:n.676+49G>C
ENST00000542957.1:c.676+49G>C	ENSP00000445301.1:n.676+49G>C
NM_001160124.1:c.550+175G>C	NP_001153596.1:n.550+175G>C
NM_001160125.1:c.676+49G>C	NP_001153597.1:n.676+49G>C
NM_001300.5:c.676+49G>C	NP_001291.3:n.676+49G>C
NR_027653.1:n.789+203G>C
NM_001300.6:c.676+49G>C MANE Select	NP_001291.3:n.676+49G>C
NM_001160124.2:c.550+175G>C	NP_001153596.1:n.550+175G>C
NR_027653.2:n.717+203G>C
NM_001160125.2:c.676+49G>C	NP_001153597.1:n.676+49G>C