Canonical Allele Identifier: CA2740044988
Gene: SAT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.23783344A>C , CM000685.2:g.23783344A>C GRCh38
NC_000023.10:g.23801461A>C , CM000685.1:g.23801461A>C GRCh37
NC_000023.9:g.23711382A>C NCBI36
NG_012929.1:g.5187A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000379270.5:c.-8A>C MANE Select ENSP00000368572.4:n.-8A>C
ENST00000683890.1:c.67A>C ENSP00000506989.1:p.Arg23=
ENST00000379251.7:c.-8A>C ENSP00000368553.3:n.-8A>C
ENST00000379253.7:c.-8A>C ENSP00000368555.3:n.-8A>C
ENST00000379254.5:c.-8A>C ENSP00000368556.1:n.-8A>C
ENST00000379270.4:c.-8A>C ENSP00000368572.4:n.-8A>C
ENST00000463236.5:n.8A>C
ENST00000489394.5:n.148A>C
NM_002970.3:c.-8A>C NP_002961.1:n.-8A>C
NR_027783.2:n.187A>C
XM_024452421.1:c.-1347A>C XP_024308189.1:n.-1347A>C
NM_002970.4:c.-8A>C MANE Select NP_002961.1:n.-8A>C
NR_027783.3:n.172A>C