Canonical Allele Identifier: CA1148773435

Gene: AGRN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1043998G= , CM000663.2:g.1043998G=	GRCh38
NC_000001.10:g.979378G= , CM000663.1:g.979378G=	GRCh37
NC_000001.9:g.969241G=	NCBI36
NG_016346.1:g.28876G= , LRG_198:g.28876G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.1974G= MANE Select	ENSP00000368678.2:p.Glu658=
ENST00000651234.1:c.1659G=	ENSP00000499046.1:p.Glu553=
ENST00000652369.1:c.1659G=	ENSP00000498543.1:p.Glu553=
ENST00000379370.6:c.1974G=	ENSP00000368678.2:p.Glu658=
ENST00000620552.4:c.1560G=	ENSP00000484607.1:p.Glu520=
NM_001305275.1:c.1974G=	NP_001292204.1:p.Glu658=
NM_198576.3:c.1974G=	NP_940978.2:p.Glu658=
XM_005244749.2:c.1974G=	XP_005244806.1:p.Glu658=
XM_006710635.2:c.1974G=	XP_006710698.1:p.Glu658=
XM_011541429.1:c.1974G=	XP_011539731.1:p.Glu658=
XM_011541430.1:c.1101G=	XP_011539732.1:p.Glu367=
XM_011541431.1:c.240G=	XP_011539733.1:p.Glu80=
XR_946650.1:n.2041G=
NM_001364727.1:c.1659G=	NP_001351656.1:p.Glu553=
XM_005244749.3:c.1974G=	XP_005244806.1:p.Glu658=
XM_011541429.2:c.1974G=	XP_011539731.1:p.Glu658=
XR_946650.2:n.2045G=
NM_001305275.2:c.1974G=	NP_001292204.1:p.Glu658=
NM_198576.4:c.1974G= MANE Select	NP_940978.2:p.Glu658=
NM_001364727.2:c.1659G=	NP_001351656.1:p.Glu553=