Canonical Allele Identifier: CA1148802037

Gene: AGRN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1047834C= , CM000663.2:g.1047834C=	GRCh38
NC_000001.10:g.983214C= , CM000663.1:g.983214C=	GRCh37
NC_000001.9:g.973077C=	NCBI36
NG_016346.1:g.32712C= , LRG_198:g.32712C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.3690C= MANE Select	ENSP00000368678.2:p.Ser1230=
ENST00000651234.1:c.3375C=	ENSP00000499046.1:p.Ser1125=
ENST00000652369.1:c.3375C=	ENSP00000498543.1:p.Ser1125=
ENST00000379370.6:c.3690C=	ENSP00000368678.2:p.Ser1230=
ENST00000466223.1:n.428C=
ENST00000478677.1:n.272C=
ENST00000620552.4:c.3276C=	ENSP00000484607.1:p.Ser1092=
NM_001305275.1:c.3690C=	NP_001292204.1:p.Ser1230=
NM_198576.3:c.3690C=	NP_940978.2:p.Ser1230=
XM_005244749.2:c.3690C=	XP_005244806.1:p.Ser1230=
XM_006710635.2:c.3690C=	XP_006710698.1:p.Ser1230=
XM_011541429.1:c.3690C=	XP_011539731.1:p.Ser1230=
XM_011541430.1:c.2817C=	XP_011539732.1:p.Ser939=
XM_011541431.1:c.1956C=	XP_011539733.1:p.Ser652=
XR_946650.1:n.3757C=
NM_001364727.1:c.3375C=	NP_001351656.1:p.Ser1125=
XM_005244749.3:c.3690C=	XP_005244806.1:p.Ser1230=
XM_011541429.2:c.3690C=	XP_011539731.1:p.Ser1230=
XR_946650.2:n.3761C=
NM_001305275.2:c.3690C=	NP_001292204.1:p.Ser1230=
NM_198576.4:c.3690C= MANE Select	NP_940978.2:p.Ser1230=
NM_001364727.2:c.3375C=	NP_001351656.1:p.Ser1125=