Canonical Allele Identifier: CA1148748121

Gene: AGRN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1040910G= , CM000663.2:g.1040910G=	GRCh38
NC_000001.10:g.976290G= , CM000663.1:g.976290G=	GRCh37
NC_000001.9:g.966153G=	NCBI36
NG_016346.1:g.25788G= , LRG_198:g.25788G=

Transcript Alleles

HGVS	Amino-acid Change
NM_198576.4:c.727+30G= MANE Select	NP_940978.2:n.727+30G=
ENST00000379370.7:c.727+30G= MANE Select	ENSP00000368678.2:n.727+30G=
NM_001305275.1:c.727+30G=	NP_001292204.1:n.727+30G=
NM_001305275.2:c.727+30G=	NP_001292204.1:n.727+30G=
NM_001364727.1:c.412+30G=	NP_001351656.1:n.412+30G=
NM_001364727.2:c.412+30G=	NP_001351656.1:n.412+30G=
NM_198576.3:c.727+30G=	NP_940978.2:n.727+30G=
ENST00000379370.6:c.727+30G=	ENSP00000368678.2:n.727+30G=
ENST00000469403.1:n.674+30G=
ENST00000620552.4:c.313+30G=	ENSP00000484607.1:n.313+30G=
ENST00000651234.1:c.412+30G=	ENSP00000499046.1:n.412+30G=
ENST00000652369.1:c.412+30G=	ENSP00000498543.1:n.412+30G=
XM_005244749.2:c.727+30G=	XP_005244806.1:n.727+30G=
XM_005244749.3:c.727+30G=	XP_005244806.1:n.727+30G=
XM_006710635.2:c.727+30G=	XP_006710698.1:n.727+30G=
XM_011541429.1:c.727+30G=	XP_011539731.1:n.727+30G=
XM_011541429.2:c.727+30G=	XP_011539731.1:n.727+30G=
XM_011541430.1:c.512-2329G=	XP_011539732.1:n.512-2329G=
XR_946650.1:n.794+30G=
XR_946650.2:n.798+30G=