Canonical Allele Identifier: CA1335698089

Gene: SAG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233346822T= , CM000664.2:g.233346822T=	GRCh38
NC_000002.11:g.234255468T= , CM000664.1:g.234255468T=	GRCh37
NC_000002.10:g.233920207T=	NCBI36
NG_009116.1:g.44160T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000409110.6:c.1128T= MANE Select	ENSP00000386444.1:p.Asn376=
ENST00000409110.5:c.1128T=	ENSP00000386444.1:p.Asn376=
ENST00000412969.6:n.2348T=
ENST00000471884.5:n.3159T=
ENST00000474220.5:n.334T=
ENST00000476500.5:n.6427T=
ENST00000492629.1:n.89T=
NM_000541.4:c.1128T=	NP_000532.2:p.Asn376=
XM_011511589.1:c.1128T=	XP_011509891.1:p.Asn376=
XM_011511590.1:c.1128T=	XP_011509892.1:p.Asn376=
XM_011511591.1:c.1118T=	XP_011509893.1:p.Ile373=
XM_011511592.1:c.972T=	XP_011509894.1:p.Asn324=
XM_011511593.1:c.828T=	XP_011509895.1:p.Asn276=
XM_011511594.1:c.756T=	XP_011509896.1:p.Asn252=
XM_011511596.1:c.726T=	XP_011509898.1:p.Asn242=
XM_011511597.1:c.726T=	XP_011509899.1:p.Asn242=
XR_922978.1:n.1445T=
XR_922979.1:n.1449T=
XR_922980.1:n.1544T=
XM_011511593.3:c.828T=	XP_011509895.1:p.Asn276=
XM_017004641.1:c.1118T=	XP_016860130.1:p.Ile373=
XM_024453036.1:c.716T=	XP_024308804.1:p.Ile239=
XR_001738882.1:n.1326T=
XR_922980.2:n.1544T=
NM_000541.5:c.1128T= MANE Select	NP_000532.2:p.Asn376=