Canonical Allele Identifier: CA2250694201
Gene: SREBF1 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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