Canonical Allele Identifier: CA2636391109

Gene: SREBF1

Linked Data

• gnomAD v4: 17-17811688-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17811688G>A , CM000679.2:g.17811688G>A	GRCh38
NC_000017.10:g.17715002G>A , CM000679.1:g.17715002G>A	GRCh37
NC_000017.9:g.17655727G>A	NCBI36
NG_007101.2:g.135216G>A
NG_029029.1:g.30324C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000261646.11:c.*934C>T MANE Select	ENSP00000261646.5:n.*934C>T
ENST00000261646.10:c.*934C>T	ENSP00000261646.5:n.*934C>T
ENST00000395757.6:c.*67C>T	ENSP00000379106.2:n.*67C>T
ENST00000485080.6:c.440C>T	ENSP00000466643.1:n.440C>T
ENST00000578469.1:c.256C>T
NM_001005291.2:c.*934C>T	NP_001005291.1:n.*934C>T
NM_004176.4:c.*934C>T	NP_004167.3:n.*934C>T
XM_005256772.3:c.*934C>T	XP_005256829.1:n.*934C>T
XM_006721570.2:c.*934C>T	XP_006721633.1:n.*934C>T
XM_011523998.1:c.*934C>T	XP_011522300.1:n.*934C>T
XM_011523999.1:c.*934C>T	XP_011522301.1:n.*934C>T
XR_429821.2:n.4390C>T
XM_024450895.1:c.*349C>T	XP_024306663.1:n.*349C>T
XR_002958058.1:n.3682C>T
NM_001005291.3:c.*934C>T	NP_001005291.1:n.*934C>T
NM_001321096.3:c.*934C>T	NP_001308025.1:n.*934C>T
NM_001388385.1:c.*934C>T	NP_001375314.1:n.*934C>T
NM_001388386.1:c.*759C>T	NP_001375315.1:n.*759C>T
NM_001388387.1:c.*934C>T	NP_001375316.1:n.*934C>T
NM_001388388.1:c.*759C>T	NP_001375317.1:n.*759C>T
NM_001388389.1:c.*934C>T	NP_001375318.1:n.*934C>T
NM_001388390.1:c.*934C>T	NP_001375319.1:n.*934C>T
NM_001388391.1:c.*934C>T	NP_001375320.1:n.*934C>T
NM_001388392.1:c.*934C>T	NP_001375321.1:n.*934C>T
NM_001388393.1:c.*934C>T	NP_001375322.1:n.*934C>T
NM_001388394.1:c.*934C>T	NP_001375323.1:n.*934C>T
NM_004176.5:c.*934C>T MANE Select	NP_004167.3:n.*934C>T
NR_170943.1:n.4359C>T
NR_170944.1:n.3564C>T
NR_170945.1:n.3654C>T
NR_170990.1:n.3510C>T