Canonical Allele Identifier: CA337834359

Gene: AGRN

Linked Data

• dbSNP Id: rs1347015442
• gnomAD v2: 1-979215-A-T
• gnomAD v4: 1-1043835-A-T
• MyVariant Identifiers: chr1:g.979215A>T (hg19) ; chr1:g.1043835A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1043835A>T , CM000663.2:g.1043835A>T	GRCh38
NC_000001.10:g.979215A>T , CM000663.1:g.979215A>T	GRCh37
NC_000001.9:g.969078A>T	NCBI36
NG_016346.1:g.28713A>T , LRG_198:g.28713A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.1811A>T MANE Select	ENSP00000368678.2:p.Asp604Val
ENST00000651234.1:c.1496A>T	ENSP00000499046.1:p.Asp499Val
ENST00000652369.1:c.1496A>T	ENSP00000498543.1:p.Asp499Val
ENST00000379370.6:c.1811A>T	ENSP00000368678.2:p.Asp604Val
ENST00000620552.4:c.1397A>T	ENSP00000484607.1:p.Asp466Val
NM_001305275.1:c.1811A>T	NP_001292204.1:p.Asp604Val
NM_198576.3:c.1811A>T	NP_940978.2:p.Asp604Val
XM_005244749.2:c.1811A>T	XP_005244806.1:p.Asp604Val
XM_006710635.2:c.1811A>T	XP_006710698.1:p.Asp604Val
XM_011541429.1:c.1811A>T	XP_011539731.1:p.Asp604Val
XM_011541430.1:c.938A>T	XP_011539732.1:p.Asp313Val
XM_011541431.1:c.77A>T	XP_011539733.1:p.Asp26Val
XR_946650.1:n.1878A>T
NM_001364727.1:c.1496A>T	NP_001351656.1:p.Asp499Val
XM_005244749.3:c.1811A>T	XP_005244806.1:p.Asp604Val
XM_011541429.2:c.1811A>T	XP_011539731.1:p.Asp604Val
XR_946650.2:n.1882A>T
NM_001305275.2:c.1811A>T	NP_001292204.1:p.Asp604Val
NM_198576.4:c.1811A>T MANE Select	NP_940978.2:p.Asp604Val
NM_001364727.2:c.1496A>T	NP_001351656.1:p.Asp499Val