Canonical Allele Identifier: CA2740044926
Gene: SAT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.23783305A>G , CM000685.2:g.23783305A>G GRCh38
NC_000023.10:g.23801422A>G , CM000685.1:g.23801422A>G GRCh37
NC_000023.9:g.23711343A>G NCBI36
NG_012929.1:g.5148A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000379270.5:c.-47A>G MANE Select ENSP00000368572.4:n.-47A>G
ENST00000683890.1:c.28A>G ENSP00000506989.1:p.Lys10Glu
ENST00000379251.7:c.-47A>G ENSP00000368553.3:n.-47A>G
ENST00000379253.7:c.-47A>G ENSP00000368555.3:n.-47A>G
ENST00000379254.5:c.-47A>G ENSP00000368556.1:n.-47A>G
ENST00000379270.4:c.-47A>G ENSP00000368572.4:n.-47A>G
ENST00000489394.5:n.109A>G
NM_002970.3:c.-47A>G NP_002961.1:n.-47A>G
NR_027783.2:n.148A>G
XM_024452421.1:c.-1386A>G XP_024308189.1:n.-1386A>G
NM_002970.4:c.-47A>G MANE Select NP_002961.1:n.-47A>G
NR_027783.3:n.133A>G