Canonical Allele Identifier: CA1335698098

Gene: SAG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233346846C= , CM000664.2:g.233346846C=	GRCh38
NC_000002.11:g.234255492C= , CM000664.1:g.234255492C=	GRCh37
NC_000002.10:g.233920231C=	NCBI36
NG_009116.1:g.44184C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409110.6:c.1152C= MANE Select	ENSP00000386444.1:p.Arg384=
ENST00000409110.5:c.1152C=	ENSP00000386444.1:p.Arg384=
ENST00000412969.6:n.2372C=
ENST00000471884.5:n.3183C=
ENST00000474220.5:n.358C=
ENST00000476500.5:n.6451C=
ENST00000492629.1:n.113C=
NM_000541.4:c.1152C=	NP_000532.2:p.Arg384=
XM_011511589.1:c.1152C=	XP_011509891.1:p.Arg384=
XM_011511590.1:c.1152C=	XP_011509892.1:p.Arg384=
XM_011511591.1:c.*20C=	XP_011509893.1:n.*20C=
XM_011511592.1:c.996C=	XP_011509894.1:p.Arg332=
XM_011511593.1:c.852C=	XP_011509895.1:p.Arg284=
XM_011511594.1:c.780C=	XP_011509896.1:p.Arg260=
XM_011511596.1:c.750C=	XP_011509898.1:p.Arg250=
XM_011511597.1:c.750C=	XP_011509899.1:p.Arg250=
XR_922978.1:n.1469C=
XR_922979.1:n.1473C=
XR_922980.1:n.1568C=
XM_011511593.3:c.852C=	XP_011509895.1:p.Arg284=
XM_017004641.1:c.*20C=	XP_016860130.1:n.*20C=
XM_024453036.1:c.*20C=	XP_024308804.1:n.*20C=
XR_001738882.1:n.1350C=
XR_922980.2:n.1568C=
NM_000541.5:c.1152C= MANE Select	NP_000532.2:p.Arg384=