Canonical Allele Identifier: CA337812203

Gene: AGRN

Linked Data

• ClinVar Variation Id: 660579
• ClinVar RCV Id: RCV000817800
• dbSNP Id: rs1570131308
• MyVariant Identifiers: chr1:g.957611G>A (hg19) ; chr1:g.1022231G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1022231G>A , CM000663.2:g.1022231G>A	GRCh38
NC_000001.10:g.957611G>A , CM000663.1:g.957611G>A	GRCh37
NC_000001.9:g.947474G>A	NCBI36
NG_016346.1:g.7109G>A , LRG_198:g.7109G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000379370.7:c.232G>A MANE Select	ENSP00000368678.2:p.Asp78Asn
ENST00000379370.6:c.232G>A	ENSP00000368678.2:p.Asp78Asn
ENST00000620552.4:c.-183G>A	ENSP00000484607.1:n.-183G>A
NM_001305275.1:c.232G>A	NP_001292204.1:p.Asp78Asn
NM_198576.3:c.232G>A	NP_940978.2:p.Asp78Asn
XM_005244749.2:c.232G>A	XP_005244806.1:p.Asp78Asn
XM_006710635.2:c.232G>A	XP_006710698.1:p.Asp78Asn
XM_011541429.1:c.232G>A	XP_011539731.1:p.Asp78Asn
XM_011541430.1:c.232G>A	XP_011539732.1:p.Asp78Asn
XR_946650.1:n.299G>A
XM_005244749.3:c.232G>A	XP_005244806.1:p.Asp78Asn
XM_011541429.2:c.232G>A	XP_011539731.1:p.Asp78Asn
XR_946650.2:n.303G>A
NM_001305275.2:c.232G>A	NP_001292204.1:p.Asp78Asn
NM_198576.4:c.232G>A MANE Select	NP_940978.2:p.Asp78Asn