Canonical Allele Identifier: CA337847628

Gene: AGRN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1046679G>A , CM000663.2:g.1046679G>A	GRCh38
NC_000001.10:g.982059G>A , CM000663.1:g.982059G>A	GRCh37
NC_000001.9:g.971922G>A	NCBI36
NG_016346.1:g.31557G>A , LRG_198:g.31557G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.3194G>A MANE Select	ENSP00000368678.2:p.Gly1065Glu
ENST00000651234.1:c.2879G>A	ENSP00000499046.1:p.Gly960Glu
ENST00000652369.1:c.2879G>A	ENSP00000498543.1:p.Gly960Glu
ENST00000379370.6:c.3194G>A	ENSP00000368678.2:p.Gly1065Glu
ENST00000620552.4:c.2780G>A	ENSP00000484607.1:p.Gly927Glu
NM_001305275.1:c.3194G>A	NP_001292204.1:p.Gly1065Glu
NM_198576.3:c.3194G>A	NP_940978.2:p.Gly1065Glu
XM_005244749.2:c.3194G>A	XP_005244806.1:p.Gly1065Glu
XM_006710635.2:c.3194G>A	XP_006710698.1:p.Gly1065Glu
XM_011541429.1:c.3194G>A	XP_011539731.1:p.Gly1065Glu
XM_011541430.1:c.2321G>A	XP_011539732.1:p.Gly774Glu
XM_011541431.1:c.1460G>A	XP_011539733.1:p.Gly487Glu
XR_946650.1:n.3261G>A
NM_001364727.1:c.2879G>A	NP_001351656.1:p.Gly960Glu
XM_005244749.3:c.3194G>A	XP_005244806.1:p.Gly1065Glu
XM_011541429.2:c.3194G>A	XP_011539731.1:p.Gly1065Glu
XR_946650.2:n.3265G>A
NM_001305275.2:c.3194G>A	NP_001292204.1:p.Gly1065Glu
NM_198576.4:c.3194G>A MANE Select	NP_940978.2:p.Gly1065Glu
NM_001364727.2:c.2879G>A	NP_001351656.1:p.Gly960Glu