Canonical Allele Identifier: CA1148804945

Gene: AGRN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1048233G= , CM000663.2:g.1048233G=	GRCh38
NC_000001.10:g.983613G= , CM000663.1:g.983613G=	GRCh37
NC_000001.9:g.973476G=	NCBI36
NG_016346.1:g.33111G= , LRG_198:g.33111G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.3973G= MANE Select	ENSP00000368678.2:p.Ala1325=
ENST00000651234.1:c.3658G=	ENSP00000499046.1:p.Ala1220=
ENST00000652369.1:c.3658G=	ENSP00000498543.1:p.Ala1220=
ENST00000379370.6:c.3973G=	ENSP00000368678.2:p.Ala1325=
ENST00000620552.4:c.3559G=	ENSP00000484607.1:p.Ala1187=
NM_001305275.1:c.3973G=	NP_001292204.1:p.Ala1325=
NM_198576.3:c.3973G=	NP_940978.2:p.Ala1325=
XM_005244749.2:c.3973G=	XP_005244806.1:p.Ala1325=
XM_006710635.2:c.3973G=	XP_006710698.1:p.Ala1325=
XM_011541429.1:c.3973G=	XP_011539731.1:p.Ala1325=
XM_011541430.1:c.3100G=	XP_011539732.1:p.Ala1034=
XM_011541431.1:c.2239G=	XP_011539733.1:p.Ala747=
XR_946650.1:n.4040G=
NM_001364727.1:c.3658G=	NP_001351656.1:p.Ala1220=
XM_005244749.3:c.3973G=	XP_005244806.1:p.Ala1325=
XM_011541429.2:c.3973G=	XP_011539731.1:p.Ala1325=
XR_946650.2:n.4044G=
NM_001305275.2:c.3973G=	NP_001292204.1:p.Ala1325=
NM_198576.4:c.3973G= MANE Select	NP_940978.2:p.Ala1325=
NM_001364727.2:c.3658G=	NP_001351656.1:p.Ala1220=