Canonical Allele Identifier: CA510320

Gene: AGRN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1054897G>A , CM000663.2:g.1054897G>A	GRCh38
NC_000001.10:g.990277G>A , CM000663.1:g.990277G>A	GRCh37
NC_000001.9:g.980140G>A	NCBI36
NG_016346.1:g.39775G>A , LRG_198:g.39775G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.6054G>A MANE Select	ENSP00000368678.2:p.Arg2018=
ENST00000651234.1:c.5808G>A	ENSP00000499046.1:p.Arg1936=
ENST00000652369.1:c.5739G>A	ENSP00000498543.1:p.Arg1913=
ENST00000379370.6:c.6054G>A	ENSP00000368678.2:p.Arg2018=
ENST00000461111.1:n.2170G>A
ENST00000620552.4:c.5709G>A	ENSP00000484607.1:p.Arg1903=
NM_001305275.1:c.6123G>A	NP_001292204.1:p.Arg2041=
NM_198576.3:c.6054G>A	NP_940978.2:p.Arg2018=
XM_005244749.2:c.6066G>A	XP_005244806.1:p.Arg2022=
XM_011541429.1:c.5992+346G>A	XP_011539731.1:n.5992+346G>A
XM_011541430.1:c.5193G>A	XP_011539732.1:p.Arg1731=
XM_011541431.1:c.4332G>A	XP_011539733.1:p.Arg1444=
XR_946650.1:n.6133G>A
NM_001364727.1:c.5751G>A	NP_001351656.1:p.Arg1917=
XM_005244749.3:c.6066G>A	XP_005244806.1:p.Arg2022=
XM_011541429.2:c.5992+346G>A	XP_011539731.1:n.5992+346G>A
XR_946650.2:n.6137G>A
NM_001305275.2:c.6123G>A	NP_001292204.1:p.Arg2041=
NM_198576.4:c.6054G>A MANE Select	NP_940978.2:p.Arg2018=
NM_001364727.2:c.5751G>A	NP_001351656.1:p.Arg1917=