Canonical Allele Identifier: CA1148772204

Gene: AGRN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1043850T= , CM000663.2:g.1043850T=	GRCh38
NC_000001.10:g.979230T= , CM000663.1:g.979230T=	GRCh37
NC_000001.9:g.969093T=	NCBI36
NG_016346.1:g.28728T= , LRG_198:g.28728T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.1826T= MANE Select	ENSP00000368678.2:p.Phe609=
ENST00000651234.1:c.1511T=	ENSP00000499046.1:p.Phe504=
ENST00000652369.1:c.1511T=	ENSP00000498543.1:p.Phe504=
ENST00000379370.6:c.1826T=	ENSP00000368678.2:p.Phe609=
ENST00000620552.4:c.1412T=	ENSP00000484607.1:p.Phe471=
NM_001305275.1:c.1826T=	NP_001292204.1:p.Phe609=
NM_198576.3:c.1826T=	NP_940978.2:p.Phe609=
XM_005244749.2:c.1826T=	XP_005244806.1:p.Phe609=
XM_006710635.2:c.1826T=	XP_006710698.1:p.Phe609=
XM_011541429.1:c.1826T=	XP_011539731.1:p.Phe609=
XM_011541430.1:c.953T=	XP_011539732.1:p.Phe318=
XM_011541431.1:c.92T=	XP_011539733.1:p.Phe31=
XR_946650.1:n.1893T=
NM_001364727.1:c.1511T=	NP_001351656.1:p.Phe504=
XM_005244749.3:c.1826T=	XP_005244806.1:p.Phe609=
XM_011541429.2:c.1826T=	XP_011539731.1:p.Phe609=
XR_946650.2:n.1897T=
NM_001305275.2:c.1826T=	NP_001292204.1:p.Phe609=
NM_198576.4:c.1826T= MANE Select	NP_940978.2:p.Phe609=
NM_001364727.2:c.1511T=	NP_001351656.1:p.Phe504=