Canonical Allele Identifier: CA509209
Gene: AGRN HGNC NCBI

Linked Data

dbSNP Id: rs780934260
gnomAD v2: 1-983282-G-T
gnomAD v3: 1-1047902-G-T
gnomAD v4: 1-1047902-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1047902G>T , CM000663.2:g.1047902G>T GRCh38
NC_000001.10:g.983282G>T , CM000663.1:g.983282G>T GRCh37
NC_000001.9:g.973145G>T NCBI36
NG_016346.1:g.32780G>T , LRG_198:g.32780G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000379370.7:c.3751+7G>T MANE Select ENSP00000368678.2:n.3751+7G>T
ENST00000651234.1:c.3436+7G>T ENSP00000499046.1:n.3436+7G>T
ENST00000652369.1:c.3436+7G>T ENSP00000498543.1:n.3436+7G>T
ENST00000379370.6:c.3751+7G>T ENSP00000368678.2:n.3751+7G>T
ENST00000620552.4:c.3337+7G>T ENSP00000484607.1:n.3337+7G>T
NM_001305275.1:c.3751+7G>T NP_001292204.1:n.3751+7G>T
NM_198576.3:c.3751+7G>T NP_940978.2:n.3751+7G>T
XM_005244749.2:c.3751+7G>T XP_005244806.1:n.3751+7G>T
XM_006710635.2:c.3751+7G>T XP_006710698.1:n.3751+7G>T
XM_011541429.1:c.3751+7G>T XP_011539731.1:n.3751+7G>T
XM_011541430.1:c.2878+7G>T XP_011539732.1:n.2878+7G>T
XM_011541431.1:c.2017+7G>T XP_011539733.1:n.2017+7G>T
XR_946650.1:n.3818+7G>T
NM_001364727.1:c.3436+7G>T NP_001351656.1:n.3436+7G>T
XM_005244749.3:c.3751+7G>T XP_005244806.1:n.3751+7G>T
XM_011541429.2:c.3751+7G>T XP_011539731.1:n.3751+7G>T
XR_946650.2:n.3822+7G>T
NM_001305275.2:c.3751+7G>T NP_001292204.1:n.3751+7G>T
NM_198576.4:c.3751+7G>T MANE Select NP_940978.2:n.3751+7G>T
NM_001364727.2:c.3436+7G>T NP_001351656.1:n.3436+7G>T