Canonical Allele Identifier: CA2510733897
Gene: AGRN HGNC NCBI

Linked Data

gnomAD v4: 1-1047952-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1047952G>A , CM000663.2:g.1047952G>A GRCh38
NC_000001.10:g.983332G>A , CM000663.1:g.983332G>A GRCh37
NC_000001.9:g.973195G>A NCBI36
NG_016346.1:g.32830G>A , LRG_198:g.32830G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000379370.7:c.3751+57G>A MANE Select ENSP00000368678.2:n.3751+57G>A
ENST00000651234.1:c.3436+57G>A ENSP00000499046.1:n.3436+57G>A
ENST00000652369.1:c.3436+57G>A ENSP00000498543.1:n.3436+57G>A
ENST00000379370.6:c.3751+57G>A ENSP00000368678.2:n.3751+57G>A
ENST00000620552.4:c.3337+57G>A ENSP00000484607.1:n.3337+57G>A
NM_001305275.1:c.3751+57G>A NP_001292204.1:n.3751+57G>A
NM_198576.3:c.3751+57G>A NP_940978.2:n.3751+57G>A
XM_005244749.2:c.3751+57G>A XP_005244806.1:n.3751+57G>A
XM_006710635.2:c.3751+57G>A XP_006710698.1:n.3751+57G>A
XM_011541429.1:c.3751+57G>A XP_011539731.1:n.3751+57G>A
XM_011541430.1:c.2878+57G>A XP_011539732.1:n.2878+57G>A
XM_011541431.1:c.2017+57G>A XP_011539733.1:n.2017+57G>A
XR_946650.1:n.3818+57G>A
NM_001364727.1:c.3436+57G>A NP_001351656.1:n.3436+57G>A
XM_005244749.3:c.3751+57G>A XP_005244806.1:n.3751+57G>A
XM_011541429.2:c.3751+57G>A XP_011539731.1:n.3751+57G>A
XR_946650.2:n.3822+57G>A
NM_001305275.2:c.3751+57G>A NP_001292204.1:n.3751+57G>A
NM_198576.4:c.3751+57G>A MANE Select NP_940978.2:n.3751+57G>A
NM_001364727.2:c.3436+57G>A NP_001351656.1:n.3436+57G>A