Canonical Allele Identifier: CA1148224142

Gene: AGRN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1050763G= , CM000663.2:g.1050763G=	GRCh38
NC_000001.10:g.986143G= , CM000663.1:g.986143G=	GRCh37
NC_000001.9:g.976006G=	NCBI36
NG_016346.1:g.35641G= , LRG_198:g.35641G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.5179G= MANE Select	ENSP00000368678.2:p.Val1727=
ENST00000651234.1:c.4864G=	ENSP00000499046.1:p.Val1622=
ENST00000652369.1:c.4864G=	ENSP00000498543.1:p.Val1622=
ENST00000379370.6:c.5179G=	ENSP00000368678.2:p.Val1727=
ENST00000419249.1:c.74G=
ENST00000620552.4:c.4765G=	ENSP00000484607.1:p.Val1589=
NM_001305275.1:c.5179G=	NP_001292204.1:p.Val1727=
NM_198576.3:c.5179G=	NP_940978.2:p.Val1727=
XM_005244749.2:c.5179G=	XP_005244806.1:p.Val1727=
XM_006710635.2:c.5179G=	XP_006710698.1:p.Val1727=
XM_011541429.1:c.5179G=	XP_011539731.1:p.Val1727=
XM_011541430.1:c.4306G=	XP_011539732.1:p.Val1436=
XM_011541431.1:c.3445G=	XP_011539733.1:p.Val1149=
XR_946650.1:n.5246G=
NM_001364727.1:c.4864G=	NP_001351656.1:p.Val1622=
XM_005244749.3:c.5179G=	XP_005244806.1:p.Val1727=
XM_011541429.2:c.5179G=	XP_011539731.1:p.Val1727=
XR_946650.2:n.5250G=
NM_001305275.2:c.5179G=	NP_001292204.1:p.Val1727=
NM_198576.4:c.5179G= MANE Select	NP_940978.2:p.Val1727=
NM_001364727.2:c.4864G=	NP_001351656.1:p.Val1622=