Canonical Allele Identifier: CA2419788591
Gene: SAT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.23783329G= , CM000685.2:g.23783329G= GRCh38
NC_000023.10:g.23801446G= , CM000685.1:g.23801446G= GRCh37
NC_000023.9:g.23711367G= NCBI36
NG_012929.1:g.5172G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000379270.5:c.-23G= MANE Select ENSP00000368572.4:n.-23G=
ENST00000683890.1:c.52G= ENSP00000506989.1:p.Gly18=
ENST00000379251.7:c.-23G= ENSP00000368553.3:n.-23G=
ENST00000379253.7:c.-23G= ENSP00000368555.3:n.-23G=
ENST00000379254.5:c.-23G= ENSP00000368556.1:n.-23G=
ENST00000379270.4:c.-23G= ENSP00000368572.4:n.-23G=
ENST00000489394.5:n.133G=
NM_002970.3:c.-23G= NP_002961.1:n.-23G=
NR_027783.2:n.172G=
XM_024452421.1:c.-1362G= XP_024308189.1:n.-1362G=
NM_002970.4:c.-23G= MANE Select NP_002961.1:n.-23G=
NR_027783.3:n.157G=