Canonical Allele Identifier: CA2018025596

Gene: KLF12

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.74061451G= , CM000675.2:g.74061451G=	GRCh38
NC_000013.10:g.74635588G= , CM000675.1:g.74635588G=	GRCh37
NC_000013.9:g.73533589G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703967.1:c.-31-66398C= MANE Select	ENSP00000515592.1:n.-31-66398C=
ENST00000377669.7:c.-31-66398C=	ENSP00000366897.2:n.-31-66398C=
ENST00000377666.5:c.-106-66398C=	ENSP00000366894.5:n.-106-66398C=
NM_007249.4:c.-31-66398C=	NP_009180.3:n.-31-66398C=
XM_005266251.2:c.-31-66398C=	XP_005266308.1:n.-31-66398C=
XM_005266252.3:c.-31-66398C=	XP_005266309.1:n.-31-66398C=
XM_011534909.1:c.-31-66398C=	XP_011533211.1:n.-31-66398C=
XM_011534912.1:c.-25+72288C=	XP_011533214.1:n.-25+72288C=
XM_005266251.4:c.-31-66398C=	XP_005266308.1:n.-31-66398C=
XM_011534909.2:c.-31-66398C=	XP_011533211.1:n.-31-66398C=
XM_011534912.2:c.-25+72288C=	XP_011533214.1:n.-25+72288C=
NM_007249.5:c.-31-66398C=	NP_009180.3:n.-31-66398C=
NM_001400136.1:c.-31-66398C= MANE Select	NP_001387065.1:n.-31-66398C=
NM_001400139.1:c.-31-66398C=	NP_001387068.1:n.-31-66398C=
NM_001400146.1:c.-31-66398C=	NP_001387075.1:n.-31-66398C=
NM_001400147.1:c.-25+72521C=	NP_001387076.1:n.-25+72521C=
NM_001400148.1:c.-25+72288C=	NP_001387077.1:n.-25+72288C=
NM_001400149.1:c.-31-66398C=	NP_001387078.1:n.-31-66398C=
NM_001400150.1:c.-31-66398C=	NP_001387079.1:n.-31-66398C=
NM_001400151.1:c.-31-66398C=	NP_001387080.1:n.-31-66398C=
NM_001400152.1:c.-31-66398C=	NP_001387081.1:n.-31-66398C=
NM_001400153.1:c.-31-66398C=	NP_001387082.1:n.-31-66398C=