Canonical Allele Identifier: CA1335698106

Gene: SAG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233346866G= , CM000664.2:g.233346866G=	GRCh38
NC_000002.11:g.234255512G= , CM000664.1:g.234255512G=	GRCh37
NC_000002.10:g.233920251G=	NCBI36
NG_009116.1:g.44204G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409110.6:c.1172G= MANE Select	ENSP00000386444.1:p.Gly391=
ENST00000409110.5:c.1172G=	ENSP00000386444.1:p.Gly391=
ENST00000412969.6:n.2392G=
ENST00000471884.5:n.3203G=
ENST00000474220.5:n.378G=
ENST00000476500.5:n.6471G=
ENST00000492629.1:n.133G=
NM_000541.4:c.1172G=	NP_000532.2:p.Gly391=
XM_011511589.1:c.1172G=	XP_011509891.1:p.Gly391=
XM_011511590.1:c.1172G=	XP_011509892.1:p.Gly391=
XM_011511591.1:c.*40G=	XP_011509893.1:n.*40G=
XM_011511592.1:c.1016G=	XP_011509894.1:p.Gly339=
XM_011511593.1:c.872G=	XP_011509895.1:p.Gly291=
XM_011511594.1:c.800G=	XP_011509896.1:p.Gly267=
XM_011511596.1:c.770G=	XP_011509898.1:p.Gly257=
XM_011511597.1:c.770G=	XP_011509899.1:p.Gly257=
XR_922978.1:n.1489G=
XR_922980.1:n.1588G=
XM_011511593.3:c.872G=	XP_011509895.1:p.Gly291=
XM_017004641.1:c.*40G=	XP_016860130.1:n.*40G=
XM_024453036.1:c.*40G=	XP_024308804.1:n.*40G=
XR_001738882.1:n.1370G=
XR_922980.2:n.1588G=
NM_000541.5:c.1172G= MANE Select	NP_000532.2:p.Gly391=