Canonical Allele Identifier: CA1886882338

Gene: KLF6

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.3782046_3782048delinsTGA , CM000672.2:g.3782046_3782048delinsTGA	GRCh38
NC_000010.10:g.3824238_3824240delinsTGA , CM000672.1:g.3824238_3824240delinsTGA	GRCh37
NC_000010.9:g.3814238_3814240delinsTGA	NCBI36
NG_012277.1:g.8234_8236delinsTCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000497571.6:c.269_271delinsTCA MANE Select	ENSP00000419923.1:p.Leu90=
ENST00000173785.4:n.4_6delinsTCA
ENST00000380946.3:n.504_506delinsTCA
ENST00000469435.1:c.269_271delinsTCA	ENSP00000419079.1:p.Leu90=
ENST00000497571.5:c.269_271delinsTCA	ENSP00000419923.1:p.Leu90=
ENST00000542957.1:c.269_271delinsTCA	ENSP00000445301.1:p.Leu90=
NM_001160124.1:c.269_271delinsTCA	NP_001153596.1:p.Leu90=
NM_001160125.1:c.269_271delinsTCA	NP_001153597.1:p.Leu90=
NM_001300.5:c.269_271delinsTCA	NP_001291.3:p.Leu90=
NR_027653.1:n.536_538delinsTCA
NM_001300.6:c.269_271delinsTCA MANE Select	NP_001291.3:p.Leu90=
NM_001160124.2:c.269_271delinsTCA	NP_001153596.1:p.Leu90=
NR_027653.2:n.464_466delinsTCA
NM_001160125.2:c.269_271delinsTCA	NP_001153597.1:p.Leu90=