Canonical Allele Identifier: CA337779486

Gene: AGRN

Linked Data

• gnomAD v4: 1-1049986-G-A
• MyVariant Identifiers: chr1:g.985366G>A (hg19) ; chr1:g.1049986G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1049986G>A , CM000663.2:g.1049986G>A	GRCh38
NC_000001.10:g.985366G>A , CM000663.1:g.985366G>A	GRCh37
NC_000001.9:g.975229G>A	NCBI36
NG_016346.1:g.34864G>A , LRG_198:g.34864G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.4828G>A MANE Select	ENSP00000368678.2:p.Gly1610Ser
ENST00000651234.1:c.4513G>A	ENSP00000499046.1:p.Gly1505Ser
ENST00000652369.1:c.4513G>A	ENSP00000498543.1:p.Gly1505Ser
ENST00000379370.6:c.4828G>A	ENSP00000368678.2:p.Gly1610Ser
ENST00000620552.4:c.4414G>A	ENSP00000484607.1:p.Gly1472Ser
NM_001305275.1:c.4828G>A	NP_001292204.1:p.Gly1610Ser
NM_198576.3:c.4828G>A	NP_940978.2:p.Gly1610Ser
XM_005244749.2:c.4828G>A	XP_005244806.1:p.Gly1610Ser
XM_006710635.2:c.4828G>A	XP_006710698.1:p.Gly1610Ser
XM_011541429.1:c.4828G>A	XP_011539731.1:p.Gly1610Ser
XM_011541430.1:c.3955G>A	XP_011539732.1:p.Gly1319Ser
XM_011541431.1:c.3094G>A	XP_011539733.1:p.Gly1032Ser
XR_946650.1:n.4895G>A
NM_001364727.1:c.4513G>A	NP_001351656.1:p.Gly1505Ser
XM_005244749.3:c.4828G>A	XP_005244806.1:p.Gly1610Ser
XM_011541429.2:c.4828G>A	XP_011539731.1:p.Gly1610Ser
XR_946650.2:n.4899G>A
NM_001305275.2:c.4828G>A	NP_001292204.1:p.Gly1610Ser
NM_198576.4:c.4828G>A MANE Select	NP_940978.2:p.Gly1610Ser
NM_001364727.2:c.4513G>A	NP_001351656.1:p.Gly1505Ser