Canonical Allele Identifier: CA1148773670

Gene: AGRN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1044023G= , CM000663.2:g.1044023G=	GRCh38
NC_000001.10:g.979403G= , CM000663.1:g.979403G=	GRCh37
NC_000001.9:g.969266G=	NCBI36
NG_016346.1:g.28901G= , LRG_198:g.28901G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.1999G= MANE Select	ENSP00000368678.2:p.Ala667=
ENST00000651234.1:c.1684G=	ENSP00000499046.1:p.Ala562=
ENST00000652369.1:c.1684G=	ENSP00000498543.1:p.Ala562=
ENST00000379370.6:c.1999G=	ENSP00000368678.2:p.Ala667=
ENST00000620552.4:c.1585G=	ENSP00000484607.1:p.Ala529=
NM_001305275.1:c.1999G=	NP_001292204.1:p.Ala667=
NM_198576.3:c.1999G=	NP_940978.2:p.Ala667=
XM_005244749.2:c.1999G=	XP_005244806.1:p.Ala667=
XM_006710635.2:c.1999G=	XP_006710698.1:p.Ala667=
XM_011541429.1:c.1999G=	XP_011539731.1:p.Ala667=
XM_011541430.1:c.1126G=	XP_011539732.1:p.Ala376=
XM_011541431.1:c.265G=	XP_011539733.1:p.Ala89=
XR_946650.1:n.2066G=
NM_001364727.1:c.1684G=	NP_001351656.1:p.Ala562=
XM_005244749.3:c.1999G=	XP_005244806.1:p.Ala667=
XM_011541429.2:c.1999G=	XP_011539731.1:p.Ala667=
XR_946650.2:n.2070G=
NM_001305275.2:c.1999G=	NP_001292204.1:p.Ala667=
NM_198576.4:c.1999G= MANE Select	NP_940978.2:p.Ala667=
NM_001364727.2:c.1684G=	NP_001351656.1:p.Ala562=