Canonical Allele Identifier: CA1148804598

Gene: AGRN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1022313A= , CM000663.2:g.1022313A=	GRCh38
NC_000001.10:g.957693A= , CM000663.1:g.957693A=	GRCh37
NC_000001.9:g.947556A=	NCBI36
NG_016346.1:g.7191A= , LRG_198:g.7191A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.314A= MANE Select	ENSP00000368678.2:p.Asn105=
ENST00000379370.6:c.314A=	ENSP00000368678.2:p.Asn105=
ENST00000620552.4:c.-101A=	ENSP00000484607.1:n.-101A=
NM_001305275.1:c.314A=	NP_001292204.1:p.Asn105=
NM_198576.3:c.314A=	NP_940978.2:p.Asn105=
XM_005244749.2:c.314A=	XP_005244806.1:p.Asn105=
XM_006710635.2:c.314A=	XP_006710698.1:p.Asn105=
XM_011541429.1:c.314A=	XP_011539731.1:p.Asn105=
XM_011541430.1:c.314A=	XP_011539732.1:p.Asn105=
XR_946650.1:n.381A=
XM_005244749.3:c.314A=	XP_005244806.1:p.Asn105=
XM_011541429.2:c.314A=	XP_011539731.1:p.Asn105=
XR_946650.2:n.385A=
NM_001305275.2:c.314A=	NP_001292204.1:p.Asn105=
NM_198576.4:c.314A= MANE Select	NP_940978.2:p.Asn105=