Canonical Allele Identifier: CA1335698108

Gene: SAG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233346876G= , CM000664.2:g.233346876G=	GRCh38
NC_000002.11:g.234255522G= , CM000664.1:g.234255522G=	GRCh37
NC_000002.10:g.233920261G=	NCBI36
NG_009116.1:g.44214G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409110.6:c.1182G= MANE Select	ENSP00000386444.1:p.Glu394=
ENST00000409110.5:c.1182G=	ENSP00000386444.1:p.Glu394=
ENST00000412969.6:n.2402G=
ENST00000471884.5:n.3213G=
ENST00000474220.5:n.388G=
ENST00000476500.5:n.6481G=
ENST00000492629.1:n.143G=
NM_000541.4:c.1182G=	NP_000532.2:p.Glu394=
XM_011511589.1:c.1182G=	XP_011509891.1:p.Glu394=
XM_011511590.1:c.1182G=	XP_011509892.1:p.Glu394=
XM_011511591.1:c.*50G=	XP_011509893.1:n.*50G=
XM_011511592.1:c.1026G=	XP_011509894.1:p.Glu342=
XM_011511593.1:c.882G=	XP_011509895.1:p.Glu294=
XM_011511594.1:c.810G=	XP_011509896.1:p.Glu270=
XM_011511596.1:c.780G=	XP_011509898.1:p.Glu260=
XM_011511597.1:c.780G=	XP_011509899.1:p.Glu260=
XR_922978.1:n.1499G=
XR_922980.1:n.1598G=
XM_011511593.3:c.882G=	XP_011509895.1:p.Glu294=
XM_017004641.1:c.*50G=	XP_016860130.1:n.*50G=
XM_024453036.1:c.*50G=	XP_024308804.1:n.*50G=
XR_001738882.1:n.1380G=
XR_922980.2:n.1598G=
NM_000541.5:c.1182G= MANE Select	NP_000532.2:p.Glu394=