Canonical Allele Identifier: CA1148773549

Gene: AGRN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1044007A= , CM000663.2:g.1044007A=	GRCh38
NC_000001.10:g.979387A= , CM000663.1:g.979387A=	GRCh37
NC_000001.9:g.969250A=	NCBI36
NG_016346.1:g.28885A= , LRG_198:g.28885A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.1983A= MANE Select	ENSP00000368678.2:p.Ala661=
ENST00000651234.1:c.1668A=	ENSP00000499046.1:p.Ala556=
ENST00000652369.1:c.1668A=	ENSP00000498543.1:p.Ala556=
ENST00000379370.6:c.1983A=	ENSP00000368678.2:p.Ala661=
ENST00000620552.4:c.1569A=	ENSP00000484607.1:p.Ala523=
NM_001305275.1:c.1983A=	NP_001292204.1:p.Ala661=
NM_198576.3:c.1983A=	NP_940978.2:p.Ala661=
XM_005244749.2:c.1983A=	XP_005244806.1:p.Ala661=
XM_006710635.2:c.1983A=	XP_006710698.1:p.Ala661=
XM_011541429.1:c.1983A=	XP_011539731.1:p.Ala661=
XM_011541430.1:c.1110A=	XP_011539732.1:p.Ala370=
XM_011541431.1:c.249A=	XP_011539733.1:p.Ala83=
XR_946650.1:n.2050A=
NM_001364727.1:c.1668A=	NP_001351656.1:p.Ala556=
XM_005244749.3:c.1983A=	XP_005244806.1:p.Ala661=
XM_011541429.2:c.1983A=	XP_011539731.1:p.Ala661=
XR_946650.2:n.2054A=
NM_001305275.2:c.1983A=	NP_001292204.1:p.Ala661=
NM_198576.4:c.1983A= MANE Select	NP_940978.2:p.Ala661=
NM_001364727.2:c.1668A=	NP_001351656.1:p.Ala556=