Canonical Allele Identifier: CA375869093

Gene: KLF6

Linked Data

• COSMIC: COSM41254 ; COSM4864871
• MyVariant Identifiers: chr10:g.3824025A>C (hg19) ; chr10:g.3781833A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.3781833A>C , CM000672.2:g.3781833A>C	GRCh38
NC_000010.10:g.3824025A>C , CM000672.1:g.3824025A>C	GRCh37
NC_000010.9:g.3814025A>C	NCBI36
NG_012277.1:g.8449T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000497571.6:c.484T>G MANE Select	ENSP00000419923.1:p.Trp162Gly
ENST00000173785.4:n.219T>G
ENST00000380946.3:n.719T>G
ENST00000469435.1:c.484T>G	ENSP00000419079.1:p.Trp162Gly
ENST00000497571.5:c.484T>G	ENSP00000419923.1:p.Trp162Gly
ENST00000542957.1:c.484T>G	ENSP00000445301.1:p.Trp162Gly
NM_001160124.1:c.484T>G	NP_001153596.1:p.Trp162Gly
NM_001160125.1:c.484T>G	NP_001153597.1:p.Trp162Gly
NM_001300.5:c.484T>G	NP_001291.3:p.Trp162Gly
NR_027653.1:n.751T>G
NM_001300.6:c.484T>G MANE Select	NP_001291.3:p.Trp162Gly
NM_001160124.2:c.484T>G	NP_001153596.1:p.Trp162Gly
NR_027653.2:n.679T>G
NM_001160125.2:c.484T>G	NP_001153597.1:p.Trp162Gly