Canonical Allele Identifier: CA2250694234

Gene: SREBF1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17811720A= , CM000679.2:g.17811720A=	GRCh38
NC_000017.10:g.17715034A= , CM000679.1:g.17715034A=	GRCh37
NC_000017.9:g.17655759A=	NCBI36
NG_007101.2:g.135248A=
NG_029029.1:g.30292T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261646.11:c.*902T= MANE Select	ENSP00000261646.5:n.*902T=
ENST00000261646.10:c.*902T=	ENSP00000261646.5:n.*902T=
ENST00000395757.6:c.*35T=	ENSP00000379106.2:n.*35T=
ENST00000485080.6:c.408T=	ENSP00000466643.1:n.408T=
ENST00000578469.1:c.224T=
NM_001005291.2:c.*902T=	NP_001005291.1:n.*902T=
NM_004176.4:c.*902T=	NP_004167.3:n.*902T=
XM_005256772.3:c.*902T=	XP_005256829.1:n.*902T=
XM_006721570.2:c.*902T=	XP_006721633.1:n.*902T=
XM_011523998.1:c.*902T=	XP_011522300.1:n.*902T=
XM_011523999.1:c.*902T=	XP_011522301.1:n.*902T=
XR_429821.2:n.4358T=
XM_024450895.1:c.*317T=	XP_024306663.1:n.*317T=
XR_002958058.1:n.3650T=
NM_001005291.3:c.*902T=	NP_001005291.1:n.*902T=
NM_001321096.3:c.*902T=	NP_001308025.1:n.*902T=
NM_001388385.1:c.*902T=	NP_001375314.1:n.*902T=
NM_001388386.1:c.*727T=	NP_001375315.1:n.*727T=
NM_001388387.1:c.*902T=	NP_001375316.1:n.*902T=
NM_001388388.1:c.*727T=	NP_001375317.1:n.*727T=
NM_001388389.1:c.*902T=	NP_001375318.1:n.*902T=
NM_001388390.1:c.*902T=	NP_001375319.1:n.*902T=
NM_001388391.1:c.*902T=	NP_001375320.1:n.*902T=
NM_001388392.1:c.*902T=	NP_001375321.1:n.*902T=
NM_001388393.1:c.*902T=	NP_001375322.1:n.*902T=
NM_001388394.1:c.*902T=	NP_001375323.1:n.*902T=
NM_004176.5:c.*902T= MANE Select	NP_004167.3:n.*902T=
NR_170943.1:n.4327T=
NR_170944.1:n.3532T=
NR_170945.1:n.3622T=
NR_170990.1:n.3478T=