Canonical Allele Identifier: CA2419788606

Gene: SAT1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.23783379A= , CM000685.2:g.23783379A=	GRCh38
NC_000023.10:g.23801496A= , CM000685.1:g.23801496A=	GRCh37
NC_000023.9:g.23711417A=	NCBI36
NG_012929.1:g.5222A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000379270.5:c.28A= MANE Select	ENSP00000368572.4:p.Thr10=
ENST00000379251.7:c.28A=	ENSP00000368553.3:p.Thr10=
ENST00000379253.7:c.28A=	ENSP00000368555.3:p.Thr10=
ENST00000379254.5:c.28A=	ENSP00000368556.1:p.Thr10=
ENST00000379270.4:c.28A=	ENSP00000368572.4:p.Thr10=
ENST00000463236.5:n.43A=
ENST00000489394.5:n.183A=
NM_002970.3:c.28A=	NP_002961.1:p.Thr10=
NR_027783.2:n.222A=
XM_024452421.1:c.-1312A=	XP_024308189.1:n.-1312A=
NM_002970.4:c.28A= MANE Select	NP_002961.1:p.Thr10=
NR_027783.3:n.207A=