Canonical Allele Identifier: CA1148758874

Gene: AGRN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1051775G= , CM000663.2:g.1051775G=	GRCh38
NC_000001.10:g.987155G= , CM000663.1:g.987155G=	GRCh37
NC_000001.9:g.977018G=	NCBI36
NG_016346.1:g.36653G= , LRG_198:g.36653G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.5611G= MANE Select	ENSP00000368678.2:p.Gly1871=
ENST00000651234.1:c.5308G=	ENSP00000499046.1:p.Gly1770=
ENST00000652369.1:c.5296G=	ENSP00000498543.1:p.Gly1766=
ENST00000379370.6:c.5611G=	ENSP00000368678.2:p.Gly1871=
ENST00000419249.1:c.518G=
ENST00000620552.4:c.5209G=	ENSP00000484607.1:p.Gly1737=
NM_001305275.1:c.5623G=	NP_001292204.1:p.Gly1875=
NM_198576.3:c.5611G=	NP_940978.2:p.Gly1871=
XM_005244749.2:c.5623G=	XP_005244806.1:p.Gly1875=
XM_006710635.2:c.5623G=	XP_006710698.1:p.Gly1875=
XM_011541429.1:c.5623G=	XP_011539731.1:p.Gly1875=
XM_011541430.1:c.4750G=	XP_011539732.1:p.Gly1584=
XM_011541431.1:c.3889G=	XP_011539733.1:p.Gly1297=
XR_946650.1:n.5690G=
NM_001364727.1:c.5308G=	NP_001351656.1:p.Gly1770=
XM_005244749.3:c.5623G=	XP_005244806.1:p.Gly1875=
XM_011541429.2:c.5623G=	XP_011539731.1:p.Gly1875=
XR_946650.2:n.5694G=
NM_001305275.2:c.5623G=	NP_001292204.1:p.Gly1875=
NM_198576.4:c.5611G= MANE Select	NP_940978.2:p.Gly1871=
NM_001364727.2:c.5308G=	NP_001351656.1:p.Gly1770=