Canonical Allele Identifier: CA2642492080
Gene: AGRN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1050070_1050071insTA , CM000663.2:g.1050070_1050071insTA GRCh38
NC_000001.10:g.985450_985451insTA , CM000663.1:g.985450_985451insTA GRCh37
NC_000001.9:g.975313_975314insTA NCBI36
NG_016346.1:g.34948_34949insTA , LRG_198:g.34948_34949insTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000379370.7:c.4879+33_4879+34insTA MANE Select ENSP00000368678.2:n.4879+33_4879+34insTA
ENST00000651234.1:c.4564+33_4564+34insTA ENSP00000499046.1:n.4564+33_4564+34insTA
ENST00000652369.1:c.4564+33_4564+34insTA ENSP00000498543.1:n.4564+33_4564+34insTA
ENST00000379370.6:c.4879+33_4879+34insTA ENSP00000368678.2:n.4879+33_4879+34insTA
ENST00000620552.4:c.4465+33_4465+34insTA ENSP00000484607.1:n.4465+33_4465+34insTA
NM_001305275.1:c.4879+33_4879+34insTA NP_001292204.1:n.4879+33_4879+34insTA
NM_198576.3:c.4879+33_4879+34insTA NP_940978.2:n.4879+33_4879+34insTA
XM_005244749.2:c.4879+33_4879+34insTA XP_005244806.1:n.4879+33_4879+34insTA
XM_006710635.2:c.4879+33_4879+34insTA XP_006710698.1:n.4879+33_4879+34insTA
XM_011541429.1:c.4879+33_4879+34insTA XP_011539731.1:n.4879+33_4879+34insTA
XM_011541430.1:c.4006+33_4006+34insTA XP_011539732.1:n.4006+33_4006+34insTA
XM_011541431.1:c.3145+33_3145+34insTA XP_011539733.1:n.3145+33_3145+34insTA
XR_946650.1:n.4946+33_4946+34insTA
NM_001364727.1:c.4564+33_4564+34insTA NP_001351656.1:n.4564+33_4564+34insTA
XM_005244749.3:c.4879+33_4879+34insTA XP_005244806.1:n.4879+33_4879+34insTA
XM_011541429.2:c.4879+33_4879+34insTA XP_011539731.1:n.4879+33_4879+34insTA
XR_946650.2:n.4950+33_4950+34insTA
NM_001305275.2:c.4879+33_4879+34insTA NP_001292204.1:n.4879+33_4879+34insTA
NM_198576.4:c.4879+33_4879+34insTA MANE Select NP_940978.2:n.4879+33_4879+34insTA
NM_001364727.2:c.4564+33_4564+34insTA NP_001351656.1:n.4564+33_4564+34insTA