Canonical Allele Identifier: CA1142008312

Gene: AGRN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1044137T= , CM000663.2:g.1044137T=	GRCh38
NC_000001.10:g.979517T= , CM000663.1:g.979517T=	GRCh37
NC_000001.9:g.969380T=	NCBI36
NG_016346.1:g.29015T= , LRG_198:g.29015T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.2028T= MANE Select	ENSP00000368678.2:p.Ser676=
ENST00000651234.1:c.1713T=	ENSP00000499046.1:p.Ser571=
ENST00000652369.1:c.1713T=	ENSP00000498543.1:p.Ser571=
ENST00000379370.6:c.2028T=	ENSP00000368678.2:p.Ser676=
ENST00000620552.4:c.1614T=	ENSP00000484607.1:p.Ser538=
NM_001305275.1:c.2028T=	NP_001292204.1:p.Ser676=
NM_198576.3:c.2028T=	NP_940978.2:p.Ser676=
XM_005244749.2:c.2028T=	XP_005244806.1:p.Ser676=
XM_006710635.2:c.2028T=	XP_006710698.1:p.Ser676=
XM_011541429.1:c.2028T=	XP_011539731.1:p.Ser676=
XM_011541430.1:c.1155T=	XP_011539732.1:p.Ser385=
XM_011541431.1:c.294T=	XP_011539733.1:p.Ser98=
XR_946650.1:n.2095T=
NM_001364727.1:c.1713T=	NP_001351656.1:p.Ser571=
XM_005244749.3:c.2028T=	XP_005244806.1:p.Ser676=
XM_011541429.2:c.2028T=	XP_011539731.1:p.Ser676=
XR_946650.2:n.2099T=
NM_001305275.2:c.2028T=	NP_001292204.1:p.Ser676=
NM_198576.4:c.2028T= MANE Select	NP_940978.2:p.Ser676=
NM_001364727.2:c.1713T=	NP_001351656.1:p.Ser571=