Canonical Allele Identifier: CA1148804206

Gene: AGRN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1022214G= , CM000663.2:g.1022214G=	GRCh38
NC_000001.10:g.957594G= , CM000663.1:g.957594G=	GRCh37
NC_000001.9:g.947457G=	NCBI36
NG_016346.1:g.7092G= , LRG_198:g.7092G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.215G= MANE Select	ENSP00000368678.2:p.Arg72=
ENST00000379370.6:c.215G=	ENSP00000368678.2:p.Arg72=
ENST00000620552.4:c.-200G=	ENSP00000484607.1:n.-200G=
NM_001305275.1:c.215G=	NP_001292204.1:p.Arg72=
NM_198576.3:c.215G=	NP_940978.2:p.Arg72=
XM_005244749.2:c.215G=	XP_005244806.1:p.Arg72=
XM_006710635.2:c.215G=	XP_006710698.1:p.Arg72=
XM_011541429.1:c.215G=	XP_011539731.1:p.Arg72=
XM_011541430.1:c.215G=	XP_011539732.1:p.Arg72=
XR_946650.1:n.282G=
XM_005244749.3:c.215G=	XP_005244806.1:p.Arg72=
XM_011541429.2:c.215G=	XP_011539731.1:p.Arg72=
XR_946650.2:n.286G=
NM_001305275.2:c.215G=	NP_001292204.1:p.Arg72=
NM_198576.4:c.215G= MANE Select	NP_940978.2:p.Arg72=