Canonical Allele Identifier: CA508204

Gene: AGRN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1043361G>A , CM000663.2:g.1043361G>A	GRCh38
NC_000001.10:g.978741G>A , CM000663.1:g.978741G>A	GRCh37
NC_000001.9:g.968604G>A	NCBI36
NG_016346.1:g.28239G>A , LRG_198:g.28239G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.1507G>A MANE Select	ENSP00000368678.2:p.Gly503Ser
ENST00000651234.1:c.1192G>A	ENSP00000499046.1:p.Gly398Ser
ENST00000652369.1:c.1192G>A	ENSP00000498543.1:p.Gly398Ser
ENST00000379370.6:c.1507G>A	ENSP00000368678.2:p.Gly503Ser
ENST00000620552.4:c.1093G>A	ENSP00000484607.1:p.Gly365Ser
NM_001305275.1:c.1507G>A	NP_001292204.1:p.Gly503Ser
NM_198576.3:c.1507G>A	NP_940978.2:p.Gly503Ser
XM_005244749.2:c.1507G>A	XP_005244806.1:p.Gly503Ser
XM_006710635.2:c.1507G>A	XP_006710698.1:p.Gly503Ser
XM_011541429.1:c.1507G>A	XP_011539731.1:p.Gly503Ser
XM_011541430.1:c.634G>A	XP_011539732.1:p.Gly212Ser
XM_011541431.1:c.-228G>A	XP_011539733.1:n.-228G>A
XR_946650.1:n.1574G>A
NM_001364727.1:c.1192G>A	NP_001351656.1:p.Gly398Ser
XM_005244749.3:c.1507G>A	XP_005244806.1:p.Gly503Ser
XM_011541429.2:c.1507G>A	XP_011539731.1:p.Gly503Ser
XR_946650.2:n.1578G>A
NM_001305275.2:c.1507G>A	NP_001292204.1:p.Gly503Ser
NM_198576.4:c.1507G>A MANE Select	NP_940978.2:p.Gly503Ser
NM_001364727.2:c.1192G>A	NP_001351656.1:p.Gly398Ser