Canonical Allele Identifier: CA1148747518

Gene: AGRN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1049936A= , CM000663.2:g.1049936A=	GRCh38
NC_000001.10:g.985316A= , CM000663.1:g.985316A=	GRCh37
NC_000001.9:g.975179A=	NCBI36
NG_016346.1:g.34814A= , LRG_198:g.34814A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.4778A= MANE Select	ENSP00000368678.2:p.Gln1593=
ENST00000651234.1:c.4463A=	ENSP00000499046.1:p.Gln1488=
ENST00000652369.1:c.4463A=	ENSP00000498543.1:p.Gln1488=
ENST00000379370.6:c.4778A=	ENSP00000368678.2:p.Gln1593=
ENST00000620552.4:c.4364A=	ENSP00000484607.1:p.Gln1455=
NM_001305275.1:c.4778A=	NP_001292204.1:p.Gln1593=
NM_198576.3:c.4778A=	NP_940978.2:p.Gln1593=
XM_005244749.2:c.4778A=	XP_005244806.1:p.Gln1593=
XM_006710635.2:c.4778A=	XP_006710698.1:p.Gln1593=
XM_011541429.1:c.4778A=	XP_011539731.1:p.Gln1593=
XM_011541430.1:c.3905A=	XP_011539732.1:p.Gln1302=
XM_011541431.1:c.3044A=	XP_011539733.1:p.Gln1015=
XR_946650.1:n.4845A=
NM_001364727.1:c.4463A=	NP_001351656.1:p.Gln1488=
XM_005244749.3:c.4778A=	XP_005244806.1:p.Gln1593=
XM_011541429.2:c.4778A=	XP_011539731.1:p.Gln1593=
XR_946650.2:n.4849A=
NM_001305275.2:c.4778A=	NP_001292204.1:p.Gln1593=
NM_198576.4:c.4778A= MANE Select	NP_940978.2:p.Gln1593=
NM_001364727.2:c.4463A=	NP_001351656.1:p.Gln1488=