Canonical Allele Identifier: CA337853200

Gene: AGRN

Linked Data

• dbSNP Id: rs1262718036
• gnomAD v3: 1-1048233-G-A
• gnomAD v4: 1-1048233-G-A
• MyVariant Identifiers: chr1:g.983613G>A (hg19) ; chr1:g.1048233G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1048233G>A , CM000663.2:g.1048233G>A	GRCh38
NC_000001.10:g.983613G>A , CM000663.1:g.983613G>A	GRCh37
NC_000001.9:g.973476G>A	NCBI36
NG_016346.1:g.33111G>A , LRG_198:g.33111G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.3973G>A MANE Select	ENSP00000368678.2:p.Ala1325Thr
ENST00000651234.1:c.3658G>A	ENSP00000499046.1:p.Ala1220Thr
ENST00000652369.1:c.3658G>A	ENSP00000498543.1:p.Ala1220Thr
ENST00000379370.6:c.3973G>A	ENSP00000368678.2:p.Ala1325Thr
ENST00000620552.4:c.3559G>A	ENSP00000484607.1:p.Ala1187Thr
NM_001305275.1:c.3973G>A	NP_001292204.1:p.Ala1325Thr
NM_198576.3:c.3973G>A	NP_940978.2:p.Ala1325Thr
XM_005244749.2:c.3973G>A	XP_005244806.1:p.Ala1325Thr
XM_006710635.2:c.3973G>A	XP_006710698.1:p.Ala1325Thr
XM_011541429.1:c.3973G>A	XP_011539731.1:p.Ala1325Thr
XM_011541430.1:c.3100G>A	XP_011539732.1:p.Ala1034Thr
XM_011541431.1:c.2239G>A	XP_011539733.1:p.Ala747Thr
XR_946650.1:n.4040G>A
NM_001364727.1:c.3658G>A	NP_001351656.1:p.Ala1220Thr
XM_005244749.3:c.3973G>A	XP_005244806.1:p.Ala1325Thr
XM_011541429.2:c.3973G>A	XP_011539731.1:p.Ala1325Thr
XR_946650.2:n.4044G>A
NM_001305275.2:c.3973G>A	NP_001292204.1:p.Ala1325Thr
NM_198576.4:c.3973G>A MANE Select	NP_940978.2:p.Ala1325Thr
NM_001364727.2:c.3658G>A	NP_001351656.1:p.Ala1220Thr