Canonical Allele Identifier: CA337779491
Gene: AGRN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1049989G>C , CM000663.2:g.1049989G>C GRCh38
NC_000001.10:g.985369G>C , CM000663.1:g.985369G>C GRCh37
NC_000001.9:g.975232G>C NCBI36
NG_016346.1:g.34867G>C , LRG_198:g.34867G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000379370.7:c.4831G>C MANE Select ENSP00000368678.2:p.Ala1611Pro
ENST00000651234.1:c.4516G>C ENSP00000499046.1:p.Ala1506Pro
ENST00000652369.1:c.4516G>C ENSP00000498543.1:p.Ala1506Pro
ENST00000379370.6:c.4831G>C ENSP00000368678.2:p.Ala1611Pro
ENST00000620552.4:c.4417G>C ENSP00000484607.1:p.Ala1473Pro
NM_001305275.1:c.4831G>C NP_001292204.1:p.Ala1611Pro
NM_198576.3:c.4831G>C NP_940978.2:p.Ala1611Pro
XM_005244749.2:c.4831G>C XP_005244806.1:p.Ala1611Pro
XM_006710635.2:c.4831G>C XP_006710698.1:p.Ala1611Pro
XM_011541429.1:c.4831G>C XP_011539731.1:p.Ala1611Pro
XM_011541430.1:c.3958G>C XP_011539732.1:p.Ala1320Pro
XM_011541431.1:c.3097G>C XP_011539733.1:p.Ala1033Pro
XR_946650.1:n.4898G>C
NM_001364727.1:c.4516G>C NP_001351656.1:p.Ala1506Pro
XM_005244749.3:c.4831G>C XP_005244806.1:p.Ala1611Pro
XM_011541429.2:c.4831G>C XP_011539731.1:p.Ala1611Pro
XR_946650.2:n.4902G>C
NM_001305275.2:c.4831G>C NP_001292204.1:p.Ala1611Pro
NM_198576.4:c.4831G>C MANE Select NP_940978.2:p.Ala1611Pro
NM_001364727.2:c.4516G>C NP_001351656.1:p.Ala1506Pro