Canonical Allele Identifier: CA1335698091

Gene: SAG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233346826G= , CM000664.2:g.233346826G=	GRCh38
NC_000002.11:g.234255472G= , CM000664.1:g.234255472G=	GRCh37
NC_000002.10:g.233920211G=	NCBI36
NG_009116.1:g.44164G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409110.6:c.1132G= MANE Select	ENSP00000386444.1:p.Val378=
ENST00000409110.5:c.1132G=	ENSP00000386444.1:p.Val378=
ENST00000412969.6:n.2352G=
ENST00000471884.5:n.3163G=
ENST00000474220.5:n.338G=
ENST00000476500.5:n.6431G=
ENST00000492629.1:n.93G=
NM_000541.4:c.1132G=	NP_000532.2:p.Val378=
XM_011511589.1:c.1132G=	XP_011509891.1:p.Val378=
XM_011511590.1:c.1132G=	XP_011509892.1:p.Val378=
XM_011511591.1:c.1122G=	XP_011509893.1:p.Ter374=
XM_011511592.1:c.976G=	XP_011509894.1:p.Val326=
XM_011511593.1:c.832G=	XP_011509895.1:p.Val278=
XM_011511594.1:c.760G=	XP_011509896.1:p.Val254=
XM_011511596.1:c.730G=	XP_011509898.1:p.Val244=
XM_011511597.1:c.730G=	XP_011509899.1:p.Val244=
XR_922978.1:n.1449G=
XR_922979.1:n.1453G=
XR_922980.1:n.1548G=
XM_011511593.3:c.832G=	XP_011509895.1:p.Val278=
XM_017004641.1:c.1122G=	XP_016860130.1:p.Ter374=
XM_024453036.1:c.720G=	XP_024308804.1:p.Ter240=
XR_001738882.1:n.1330G=
XR_922980.2:n.1548G=
NM_000541.5:c.1132G= MANE Select	NP_000532.2:p.Val378=