Canonical Allele Identifier: CA2636391126

Gene: SREBF1

Linked Data

• gnomAD v4: 17-17811709-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17811709A>G , CM000679.2:g.17811709A>G	GRCh38
NC_000017.10:g.17715023A>G , CM000679.1:g.17715023A>G	GRCh37
NC_000017.9:g.17655748A>G	NCBI36
NG_007101.2:g.135237A>G
NG_029029.1:g.30303T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000261646.11:c.*913T>C MANE Select	ENSP00000261646.5:n.*913T>C
ENST00000261646.10:c.*913T>C	ENSP00000261646.5:n.*913T>C
ENST00000395757.6:c.*46T>C	ENSP00000379106.2:n.*46T>C
ENST00000485080.6:c.419T>C	ENSP00000466643.1:n.419T>C
ENST00000578469.1:c.235T>C
NM_001005291.2:c.*913T>C	NP_001005291.1:n.*913T>C
NM_004176.4:c.*913T>C	NP_004167.3:n.*913T>C
XM_005256772.3:c.*913T>C	XP_005256829.1:n.*913T>C
XM_006721570.2:c.*913T>C	XP_006721633.1:n.*913T>C
XM_011523998.1:c.*913T>C	XP_011522300.1:n.*913T>C
XM_011523999.1:c.*913T>C	XP_011522301.1:n.*913T>C
XR_429821.2:n.4369T>C
XM_024450895.1:c.*328T>C	XP_024306663.1:n.*328T>C
XR_002958058.1:n.3661T>C
NM_001005291.3:c.*913T>C	NP_001005291.1:n.*913T>C
NM_001321096.3:c.*913T>C	NP_001308025.1:n.*913T>C
NM_001388385.1:c.*913T>C	NP_001375314.1:n.*913T>C
NM_001388386.1:c.*738T>C	NP_001375315.1:n.*738T>C
NM_001388387.1:c.*913T>C	NP_001375316.1:n.*913T>C
NM_001388388.1:c.*738T>C	NP_001375317.1:n.*738T>C
NM_001388389.1:c.*913T>C	NP_001375318.1:n.*913T>C
NM_001388390.1:c.*913T>C	NP_001375319.1:n.*913T>C
NM_001388391.1:c.*913T>C	NP_001375320.1:n.*913T>C
NM_001388392.1:c.*913T>C	NP_001375321.1:n.*913T>C
NM_001388393.1:c.*913T>C	NP_001375322.1:n.*913T>C
NM_001388394.1:c.*913T>C	NP_001375323.1:n.*913T>C
NM_004176.5:c.*913T>C MANE Select	NP_004167.3:n.*913T>C
NR_170943.1:n.4338T>C
NR_170944.1:n.3543T>C
NR_170945.1:n.3633T>C
NR_170990.1:n.3489T>C