Canonical Allele Identifier: CA1148802077

Gene: AGRN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1047845C= , CM000663.2:g.1047845C=	GRCh38
NC_000001.10:g.983225C= , CM000663.1:g.983225C=	GRCh37
NC_000001.9:g.973088C=	NCBI36
NG_016346.1:g.32723C= , LRG_198:g.32723C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.3701C= MANE Select	ENSP00000368678.2:p.Ser1234=
ENST00000651234.1:c.3386C=	ENSP00000499046.1:p.Ser1129=
ENST00000652369.1:c.3386C=	ENSP00000498543.1:p.Ser1129=
ENST00000379370.6:c.3701C=	ENSP00000368678.2:p.Ser1234=
ENST00000466223.1:n.439C=
ENST00000620552.4:c.3287C=	ENSP00000484607.1:p.Ser1096=
NM_001305275.1:c.3701C=	NP_001292204.1:p.Ser1234=
NM_198576.3:c.3701C=	NP_940978.2:p.Ser1234=
XM_005244749.2:c.3701C=	XP_005244806.1:p.Ser1234=
XM_006710635.2:c.3701C=	XP_006710698.1:p.Ser1234=
XM_011541429.1:c.3701C=	XP_011539731.1:p.Ser1234=
XM_011541430.1:c.2828C=	XP_011539732.1:p.Ser943=
XM_011541431.1:c.1967C=	XP_011539733.1:p.Ser656=
XR_946650.1:n.3768C=
NM_001364727.1:c.3386C=	NP_001351656.1:p.Ser1129=
XM_005244749.3:c.3701C=	XP_005244806.1:p.Ser1234=
XM_011541429.2:c.3701C=	XP_011539731.1:p.Ser1234=
XR_946650.2:n.3772C=
NM_001305275.2:c.3701C=	NP_001292204.1:p.Ser1234=
NM_198576.4:c.3701C= MANE Select	NP_940978.2:p.Ser1234=
NM_001364727.2:c.3386C=	NP_001351656.1:p.Ser1129=