Canonical Allele Identifier: CA2419788608

Gene: SAT1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.23783385G= , CM000685.2:g.23783385G=	GRCh38
NC_000023.10:g.23801502G= , CM000685.1:g.23801502G=	GRCh37
NC_000023.9:g.23711423G=	NCBI36
NG_012929.1:g.5228G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000379270.5:c.34G= MANE Select	ENSP00000368572.4:p.Ala12=
ENST00000379251.7:c.34G=	ENSP00000368553.3:p.Ala12=
ENST00000379253.7:c.34G=	ENSP00000368555.3:p.Ala12=
ENST00000379254.5:c.34G=	ENSP00000368556.1:p.Ala12=
ENST00000379270.4:c.34G=	ENSP00000368572.4:p.Ala12=
ENST00000463236.5:n.49G=
ENST00000489394.5:n.189G=
NM_002970.3:c.34G=	NP_002961.1:p.Ala12=
NR_027783.2:n.228G=
XM_024452421.1:c.-1306G=	XP_024308189.1:n.-1306G=
NM_002970.4:c.34G= MANE Select	NP_002961.1:p.Ala12=
NR_027783.3:n.213G=