Canonical Allele Identifier: CA337851173

Gene: AGRN

Linked Data

• ClinVar Variation Id: 1490925
• ClinVar RCV Id: RCV001986154
• dbSNP Id: rs2100665678
• MyVariant Identifiers: chr1:g.983162C>A (hg19) ; chr1:g.1047782C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1047782C>A , CM000663.2:g.1047782C>A	GRCh38
NC_000001.10:g.983162C>A , CM000663.1:g.983162C>A	GRCh37
NC_000001.9:g.973025C>A	NCBI36
NG_016346.1:g.32660C>A , LRG_198:g.32660C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.3638C>A MANE Select	ENSP00000368678.2:p.Ala1213Asp
ENST00000651234.1:c.3323C>A	ENSP00000499046.1:p.Ala1108Asp
ENST00000652369.1:c.3323C>A	ENSP00000498543.1:p.Ala1108Asp
ENST00000379370.6:c.3638C>A	ENSP00000368678.2:p.Ala1213Asp
ENST00000466223.1:n.376C>A
ENST00000478677.1:n.220C>A
ENST00000620552.4:c.3224C>A	ENSP00000484607.1:p.Ala1075Asp
NM_001305275.1:c.3638C>A	NP_001292204.1:p.Ala1213Asp
NM_198576.3:c.3638C>A	NP_940978.2:p.Ala1213Asp
XM_005244749.2:c.3638C>A	XP_005244806.1:p.Ala1213Asp
XM_006710635.2:c.3638C>A	XP_006710698.1:p.Ala1213Asp
XM_011541429.1:c.3638C>A	XP_011539731.1:p.Ala1213Asp
XM_011541430.1:c.2765C>A	XP_011539732.1:p.Ala922Asp
XM_011541431.1:c.1904C>A	XP_011539733.1:p.Ala635Asp
XR_946650.1:n.3705C>A
NM_001364727.1:c.3323C>A	NP_001351656.1:p.Ala1108Asp
XM_005244749.3:c.3638C>A	XP_005244806.1:p.Ala1213Asp
XM_011541429.2:c.3638C>A	XP_011539731.1:p.Ala1213Asp
XR_946650.2:n.3709C>A
NM_001305275.2:c.3638C>A	NP_001292204.1:p.Ala1213Asp
NM_198576.4:c.3638C>A MANE Select	NP_940978.2:p.Ala1213Asp
NM_001364727.2:c.3323C>A	NP_001351656.1:p.Ala1108Asp