Canonical Allele Identifier: CA1148801949

Gene: AGRN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1047828G= , CM000663.2:g.1047828G=	GRCh38
NC_000001.10:g.983208G= , CM000663.1:g.983208G=	GRCh37
NC_000001.9:g.973071G=	NCBI36
NG_016346.1:g.32706G= , LRG_198:g.32706G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.3684G= MANE Select	ENSP00000368678.2:p.Gln1228=
ENST00000651234.1:c.3369G=	ENSP00000499046.1:p.Gln1123=
ENST00000652369.1:c.3369G=	ENSP00000498543.1:p.Gln1123=
ENST00000379370.6:c.3684G=	ENSP00000368678.2:p.Gln1228=
ENST00000466223.1:n.422G=
ENST00000478677.1:n.266G=
ENST00000620552.4:c.3270G=	ENSP00000484607.1:p.Gln1090=
NM_001305275.1:c.3684G=	NP_001292204.1:p.Gln1228=
NM_198576.3:c.3684G=	NP_940978.2:p.Gln1228=
XM_005244749.2:c.3684G=	XP_005244806.1:p.Gln1228=
XM_006710635.2:c.3684G=	XP_006710698.1:p.Gln1228=
XM_011541429.1:c.3684G=	XP_011539731.1:p.Gln1228=
XM_011541430.1:c.2811G=	XP_011539732.1:p.Gln937=
XM_011541431.1:c.1950G=	XP_011539733.1:p.Gln650=
XR_946650.1:n.3751G=
NM_001364727.1:c.3369G=	NP_001351656.1:p.Gln1123=
XM_005244749.3:c.3684G=	XP_005244806.1:p.Gln1228=
XM_011541429.2:c.3684G=	XP_011539731.1:p.Gln1228=
XR_946650.2:n.3755G=
NM_001305275.2:c.3684G=	NP_001292204.1:p.Gln1228=
NM_198576.4:c.3684G= MANE Select	NP_940978.2:p.Gln1228=
NM_001364727.2:c.3369G=	NP_001351656.1:p.Gln1123=