Canonical Allele Identifier: CA2419788570

Gene: SAT1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.23783288A= , CM000685.2:g.23783288A=	GRCh38
NC_000023.10:g.23801405A= , CM000685.1:g.23801405A=	GRCh37
NC_000023.9:g.23711326A=	NCBI36
NG_012929.1:g.5131A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379270.5:c.-64A= MANE Select	ENSP00000368572.4:n.-64A=
ENST00000683890.1:c.11A=	ENSP00000506989.1:p.His4=
ENST00000379251.7:c.-64A=	ENSP00000368553.3:n.-64A=
ENST00000379253.7:c.-64A=	ENSP00000368555.3:n.-64A=
ENST00000379254.5:c.-64A=	ENSP00000368556.1:n.-64A=
ENST00000379270.4:c.-64A=	ENSP00000368572.4:n.-64A=
ENST00000489394.5:n.92A=
NM_002970.3:c.-64A=	NP_002961.1:n.-64A=
NR_027783.2:n.131A=
XM_024452421.1:c.-1403A=	XP_024308189.1:n.-1403A=
NM_002970.4:c.-64A= MANE Select	NP_002961.1:n.-64A=
NR_027783.3:n.116A=