Canonical Allele Identifier: CA509182

Gene: AGRN

Linked Data

• ClinVar Variation Id: 2780115
• ClinVar RCV Id: RCV003746724
• dbSNP Id: rs368235925
• ExAC: 1:983190 C / A
• gnomAD v2: 1-983190-C-A
• gnomAD v3: 1-1047810-C-A
• gnomAD v4: 1-1047810-C-A
• MyVariant Identifiers: chr1:g.983190C>A (hg19) ; chr1:g.1047810C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1047810C>A , CM000663.2:g.1047810C>A	GRCh38
NC_000001.10:g.983190C>A , CM000663.1:g.983190C>A	GRCh37
NC_000001.9:g.973053C>A	NCBI36
NG_016346.1:g.32688C>A , LRG_198:g.32688C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.3666C>A MANE Select	ENSP00000368678.2:p.Ala1222=
ENST00000651234.1:c.3351C>A	ENSP00000499046.1:p.Ala1117=
ENST00000652369.1:c.3351C>A	ENSP00000498543.1:p.Ala1117=
ENST00000379370.6:c.3666C>A	ENSP00000368678.2:p.Ala1222=
ENST00000466223.1:n.404C>A
ENST00000478677.1:n.248C>A
ENST00000620552.4:c.3252C>A	ENSP00000484607.1:p.Ala1084=
NM_001305275.1:c.3666C>A	NP_001292204.1:p.Ala1222=
NM_198576.3:c.3666C>A	NP_940978.2:p.Ala1222=
XM_005244749.2:c.3666C>A	XP_005244806.1:p.Ala1222=
XM_006710635.2:c.3666C>A	XP_006710698.1:p.Ala1222=
XM_011541429.1:c.3666C>A	XP_011539731.1:p.Ala1222=
XM_011541430.1:c.2793C>A	XP_011539732.1:p.Ala931=
XM_011541431.1:c.1932C>A	XP_011539733.1:p.Ala644=
XR_946650.1:n.3733C>A
NM_001364727.1:c.3351C>A	NP_001351656.1:p.Ala1117=
XM_005244749.3:c.3666C>A	XP_005244806.1:p.Ala1222=
XM_011541429.2:c.3666C>A	XP_011539731.1:p.Ala1222=
XR_946650.2:n.3737C>A
NM_001305275.2:c.3666C>A	NP_001292204.1:p.Ala1222=
NM_198576.4:c.3666C>A MANE Select	NP_940978.2:p.Ala1222=
NM_001364727.2:c.3351C>A	NP_001351656.1:p.Ala1117=