Canonical Allele Identifier: CA2250694203
Gene: SREBF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.17811692C= , CM000679.2:g.17811692C= GRCh38
NC_000017.10:g.17715006C= , CM000679.1:g.17715006C= GRCh37
NC_000017.9:g.17655731C= NCBI36
NG_007101.2:g.135220C=
NG_029029.1:g.30320G=

Transcript Alleles

HGVS Amino-acid change
ENST00000261646.11:c.*930G= MANE Select ENSP00000261646.5:n.*930G=
ENST00000261646.10:c.*930G= ENSP00000261646.5:n.*930G=
ENST00000395757.6:c.*63G= ENSP00000379106.2:n.*63G=
ENST00000485080.6:c.436G= ENSP00000466643.1:n.436G=
ENST00000578469.1:c.252G=
NM_001005291.2:c.*930G= NP_001005291.1:n.*930G=
NM_004176.4:c.*930G= NP_004167.3:n.*930G=
XM_005256772.3:c.*930G= XP_005256829.1:n.*930G=
XM_006721570.2:c.*930G= XP_006721633.1:n.*930G=
XM_011523998.1:c.*930G= XP_011522300.1:n.*930G=
XM_011523999.1:c.*930G= XP_011522301.1:n.*930G=
XR_429821.2:n.4386G=
XM_024450895.1:c.*345G= XP_024306663.1:n.*345G=
XR_002958058.1:n.3678G=
NM_001005291.3:c.*930G= NP_001005291.1:n.*930G=
NM_001321096.3:c.*930G= NP_001308025.1:n.*930G=
NM_001388385.1:c.*930G= NP_001375314.1:n.*930G=
NM_001388386.1:c.*755G= NP_001375315.1:n.*755G=
NM_001388387.1:c.*930G= NP_001375316.1:n.*930G=
NM_001388388.1:c.*755G= NP_001375317.1:n.*755G=
NM_001388389.1:c.*930G= NP_001375318.1:n.*930G=
NM_001388390.1:c.*930G= NP_001375319.1:n.*930G=
NM_001388391.1:c.*930G= NP_001375320.1:n.*930G=
NM_001388392.1:c.*930G= NP_001375321.1:n.*930G=
NM_001388393.1:c.*930G= NP_001375322.1:n.*930G=
NM_001388394.1:c.*930G= NP_001375323.1:n.*930G=
NM_004176.5:c.*930G= MANE Select NP_004167.3:n.*930G=
NR_170943.1:n.4355G=
NR_170944.1:n.3560G=
NR_170945.1:n.3650G=
NR_170990.1:n.3506G=