Canonical Allele Identifier: CA1335698093

Gene: SAG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233346836A= , CM000664.2:g.233346836A=	GRCh38
NC_000002.11:g.234255482A= , CM000664.1:g.234255482A=	GRCh37
NC_000002.10:g.233920221A=	NCBI36
NG_009116.1:g.44174A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409110.6:c.1142A= MANE Select	ENSP00000386444.1:p.Glu381=
ENST00000409110.5:c.1142A=	ENSP00000386444.1:p.Glu381=
ENST00000412969.6:n.2362A=
ENST00000471884.5:n.3173A=
ENST00000474220.5:n.348A=
ENST00000476500.5:n.6441A=
ENST00000492629.1:n.103A=
NM_000541.4:c.1142A=	NP_000532.2:p.Glu381=
XM_011511589.1:c.1142A=	XP_011509891.1:p.Glu381=
XM_011511590.1:c.1142A=	XP_011509892.1:p.Glu381=
XM_011511591.1:c.*10A=	XP_011509893.1:n.*10A=
XM_011511592.1:c.986A=	XP_011509894.1:p.Glu329=
XM_011511593.1:c.842A=	XP_011509895.1:p.Glu281=
XM_011511594.1:c.770A=	XP_011509896.1:p.Glu257=
XM_011511596.1:c.740A=	XP_011509898.1:p.Glu247=
XM_011511597.1:c.740A=	XP_011509899.1:p.Glu247=
XR_922978.1:n.1459A=
XR_922979.1:n.1463A=
XR_922980.1:n.1558A=
XM_011511593.3:c.842A=	XP_011509895.1:p.Glu281=
XM_017004641.1:c.*10A=	XP_016860130.1:n.*10A=
XM_024453036.1:c.*10A=	XP_024308804.1:n.*10A=
XR_001738882.1:n.1340A=
XR_922980.2:n.1558A=
NM_000541.5:c.1142A= MANE Select	NP_000532.2:p.Glu381=