Canonical Allele Identifier: CA1148804134

Gene: AGRN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1048154T= , CM000663.2:g.1048154T=	GRCh38
NC_000001.10:g.983534T= , CM000663.1:g.983534T=	GRCh37
NC_000001.9:g.973397T=	NCBI36
NG_016346.1:g.33032T= , LRG_198:g.33032T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.3894T= MANE Select	ENSP00000368678.2:p.Val1298=
ENST00000651234.1:c.3579T=	ENSP00000499046.1:p.Val1193=
ENST00000652369.1:c.3579T=	ENSP00000498543.1:p.Val1193=
ENST00000379370.6:c.3894T=	ENSP00000368678.2:p.Val1298=
ENST00000620552.4:c.3480T=	ENSP00000484607.1:p.Val1160=
NM_001305275.1:c.3894T=	NP_001292204.1:p.Val1298=
NM_198576.3:c.3894T=	NP_940978.2:p.Val1298=
XM_005244749.2:c.3894T=	XP_005244806.1:p.Val1298=
XM_006710635.2:c.3894T=	XP_006710698.1:p.Val1298=
XM_011541429.1:c.3894T=	XP_011539731.1:p.Val1298=
XM_011541430.1:c.3021T=	XP_011539732.1:p.Val1007=
XM_011541431.1:c.2160T=	XP_011539733.1:p.Val720=
XR_946650.1:n.3961T=
NM_001364727.1:c.3579T=	NP_001351656.1:p.Val1193=
XM_005244749.3:c.3894T=	XP_005244806.1:p.Val1298=
XM_011541429.2:c.3894T=	XP_011539731.1:p.Val1298=
XR_946650.2:n.3965T=
NM_001305275.2:c.3894T=	NP_001292204.1:p.Val1298=
NM_198576.4:c.3894T= MANE Select	NP_940978.2:p.Val1298=
NM_001364727.2:c.3579T=	NP_001351656.1:p.Val1193=