Canonical Allele Identifier: CA2642492243
Gene: AGRN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1048288_1048289insTCAAATAG , CM000663.2:g.1048288_1048289insTCAAATAG GRCh38
NC_000001.10:g.983668_983669insTCAAATAG , CM000663.1:g.983668_983669insTCAAATAG GRCh37
NC_000001.9:g.973531_973532insTCAAATAG NCBI36
NG_016346.1:g.33166_33167insTCAAATAG , LRG_198:g.33166_33167insTCAAATAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000379370.7:c.4028_4029insTCAAATAG MANE Select ENSP00000368678.2:p.Cys1344GlnfsTer?
ENST00000651234.1:c.3713_3714insTCAAATAG ENSP00000499046.1:p.Cys1239GlnfsTer?
ENST00000652369.1:c.3713_3714insTCAAATAG ENSP00000498543.1:p.Cys1239GlnfsTer?
ENST00000379370.6:c.4028_4029insTCAAATAG ENSP00000368678.2:p.Cys1344GlnfsTer?
ENST00000620552.4:c.3614_3615insTCAAATAG ENSP00000484607.1:p.Cys1206GlnfsTer?
NM_001305275.1:c.4028_4029insTCAAATAG NP_001292204.1:p.Cys1344GlnfsTer?
NM_198576.3:c.4028_4029insTCAAATAG NP_940978.2:p.Cys1344GlnfsTer?
XM_005244749.2:c.4028_4029insTCAAATAG XP_005244806.1:p.Cys1344GlnfsTer?
XM_006710635.2:c.4028_4029insTCAAATAG XP_006710698.1:p.Cys1344GlnfsTer?
XM_011541429.1:c.4028_4029insTCAAATAG XP_011539731.1:p.Cys1344GlnfsTer?
XM_011541430.1:c.3155_3156insTCAAATAG XP_011539732.1:p.Cys1053GlnfsTer?
XM_011541431.1:c.2294_2295insTCAAATAG XP_011539733.1:p.Cys766GlnfsTer?
XR_946650.1:n.4095_4096insTCAAATAG
NM_001364727.1:c.3713_3714insTCAAATAG NP_001351656.1:p.Cys1239GlnfsTer?
XM_005244749.3:c.4028_4029insTCAAATAG XP_005244806.1:p.Cys1344GlnfsTer?
XM_011541429.2:c.4028_4029insTCAAATAG XP_011539731.1:p.Cys1344GlnfsTer?
XR_946650.2:n.4099_4100insTCAAATAG
NM_001305275.2:c.4028_4029insTCAAATAG NP_001292204.1:p.Cys1344GlnfsTer?
NM_198576.4:c.4028_4029insTCAAATAG MANE Select NP_940978.2:p.Cys1344GlnfsTer?
NM_001364727.2:c.3713_3714insTCAAATAG NP_001351656.1:p.Cys1239GlnfsTer?