Canonical Allele Identifier: CA337779370
Gene: AGRN HGNC NCBI

Linked Data

dbSNP Id: rs1406970952
gnomAD v2: 1-985309-C-T
gnomAD v3: 1-1049929-C-T
gnomAD v4: 1-1049929-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1049929C>T , CM000663.2:g.1049929C>T GRCh38
NC_000001.10:g.985309C>T , CM000663.1:g.985309C>T GRCh37
NC_000001.9:g.975172C>T NCBI36
NG_016346.1:g.34807C>T , LRG_198:g.34807C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000379370.7:c.4771C>T MANE Select ENSP00000368678.2:p.Pro1591Ser
ENST00000651234.1:c.4456C>T ENSP00000499046.1:p.Pro1486Ser
ENST00000652369.1:c.4456C>T ENSP00000498543.1:p.Pro1486Ser
ENST00000379370.6:c.4771C>T ENSP00000368678.2:p.Pro1591Ser
ENST00000620552.4:c.4357C>T ENSP00000484607.1:p.Pro1453Ser
NM_001305275.1:c.4771C>T NP_001292204.1:p.Pro1591Ser
NM_198576.3:c.4771C>T NP_940978.2:p.Pro1591Ser
XM_005244749.2:c.4771C>T XP_005244806.1:p.Pro1591Ser
XM_006710635.2:c.4771C>T XP_006710698.1:p.Pro1591Ser
XM_011541429.1:c.4771C>T XP_011539731.1:p.Pro1591Ser
XM_011541430.1:c.3898C>T XP_011539732.1:p.Pro1300Ser
XM_011541431.1:c.3037C>T XP_011539733.1:p.Pro1013Ser
XR_946650.1:n.4838C>T
NM_001364727.1:c.4456C>T NP_001351656.1:p.Pro1486Ser
XM_005244749.3:c.4771C>T XP_005244806.1:p.Pro1591Ser
XM_011541429.2:c.4771C>T XP_011539731.1:p.Pro1591Ser
XR_946650.2:n.4842C>T
NM_001305275.2:c.4771C>T NP_001292204.1:p.Pro1591Ser
NM_198576.4:c.4771C>T MANE Select NP_940978.2:p.Pro1591Ser
NM_001364727.2:c.4456C>T NP_001351656.1:p.Pro1486Ser