Canonical Allele Identifier: CA1144114687

Gene: AGRN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1050526G= , CM000663.2:g.1050526G=	GRCh38
NC_000001.10:g.985906G= , CM000663.1:g.985906G=	GRCh37
NC_000001.9:g.975769G=	NCBI36
NG_016346.1:g.35404G= , LRG_198:g.35404G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.5076G= MANE Select	ENSP00000368678.2:p.Ser1692=
ENST00000651234.1:c.4761G=	ENSP00000499046.1:p.Ser1587=
ENST00000652369.1:c.4761G=	ENSP00000498543.1:p.Ser1587=
ENST00000379370.6:c.5076G=	ENSP00000368678.2:p.Ser1692=
ENST00000620552.4:c.4662G=	ENSP00000484607.1:p.Ser1554=
NM_001305275.1:c.5076G=	NP_001292204.1:p.Ser1692=
NM_198576.3:c.5076G=	NP_940978.2:p.Ser1692=
XM_005244749.2:c.5076G=	XP_005244806.1:p.Ser1692=
XM_006710635.2:c.5076G=	XP_006710698.1:p.Ser1692=
XM_011541429.1:c.5076G=	XP_011539731.1:p.Ser1692=
XM_011541430.1:c.4203G=	XP_011539732.1:p.Ser1401=
XM_011541431.1:c.3342G=	XP_011539733.1:p.Ser1114=
XR_946650.1:n.5143G=
NM_001364727.1:c.4761G=	NP_001351656.1:p.Ser1587=
XM_005244749.3:c.5076G=	XP_005244806.1:p.Ser1692=
XM_011541429.2:c.5076G=	XP_011539731.1:p.Ser1692=
XR_946650.2:n.5147G=
NM_001305275.2:c.5076G=	NP_001292204.1:p.Ser1692=
NM_198576.4:c.5076G= MANE Select	NP_940978.2:p.Ser1692=
NM_001364727.2:c.4761G=	NP_001351656.1:p.Ser1587=