Canonical Allele Identifier: CA375869073

Gene: KLF6

Linked Data

• dbSNP Id: rs1267743907
• MyVariant Identifiers: chr10:g.3824023C>A (hg19) ; chr10:g.3781831C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.3781831C>A , CM000672.2:g.3781831C>A	GRCh38
NC_000010.10:g.3824023C>A , CM000672.1:g.3824023C>A	GRCh37
NC_000010.9:g.3814023C>A	NCBI36
NG_012277.1:g.8451G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000497571.6:c.486G>T MANE Select	ENSP00000419923.1:p.Trp162Cys
ENST00000173785.4:n.221G>T
ENST00000380946.3:n.721G>T
ENST00000469435.1:c.486G>T	ENSP00000419079.1:p.Trp162Cys
ENST00000497571.5:c.486G>T	ENSP00000419923.1:p.Trp162Cys
ENST00000542957.1:c.486G>T	ENSP00000445301.1:p.Trp162Cys
NM_001160124.1:c.486G>T	NP_001153596.1:p.Trp162Cys
NM_001160125.1:c.486G>T	NP_001153597.1:p.Trp162Cys
NM_001300.5:c.486G>T	NP_001291.3:p.Trp162Cys
NR_027653.1:n.753G>T
NM_001300.6:c.486G>T MANE Select	NP_001291.3:p.Trp162Cys
NM_001160124.2:c.486G>T	NP_001153596.1:p.Trp162Cys
NR_027653.2:n.681G>T
NM_001160125.2:c.486G>T	NP_001153597.1:p.Trp162Cys