Canonical Allele Identifier: CA2562111314
Gene: AGRN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1047750_1047751insCGGGCTCTGCC , CM000663.2:g.1047750_1047751insCGGGCTCTGCC GRCh38
NC_000001.10:g.983130_983131insCGGGCTCTGCC , CM000663.1:g.983130_983131insCGGGCTCTGCC GRCh37
NC_000001.9:g.972993_972994insCGGGCTCTGCC NCBI36
NG_016346.1:g.32628_32629insCGGGCTCTGCC , LRG_198:g.32628_32629insCGGGCTCTGCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000379370.7:c.3632-26_3632-25insCGGGCTCTGCC MANE Select ENSP00000368678.2:n.3632-26_3632-25insCGGGCTCTGCC
ENST00000651234.1:c.3317-26_3317-25insCGGGCTCTGCC ENSP00000499046.1:n.3317-26_3317-25insCGGGCTCTGCC
ENST00000652369.1:c.3317-26_3317-25insCGGGCTCTGCC ENSP00000498543.1:n.3317-26_3317-25insCGGGCTCTGCC
ENST00000379370.6:c.3632-26_3632-25insCGGGCTCTGCC ENSP00000368678.2:n.3632-26_3632-25insCGGGCTCTGCC
ENST00000466223.1:n.370-26_370-25insCGGGCTCTGCC
ENST00000478677.1:n.214-26_214-25insCGGGCTCTGCC
ENST00000620552.4:c.3218-26_3218-25insCGGGCTCTGCC ENSP00000484607.1:n.3218-26_3218-25insCGGGCTCTGCC
NM_001305275.1:c.3632-26_3632-25insCGGGCTCTGCC NP_001292204.1:n.3632-26_3632-25insCGGGCTCTGCC
NM_198576.3:c.3632-26_3632-25insCGGGCTCTGCC NP_940978.2:n.3632-26_3632-25insCGGGCTCTGCC
XM_005244749.2:c.3632-26_3632-25insCGGGCTCTGCC XP_005244806.1:n.3632-26_3632-25insCGGGCTCTGCC
XM_006710635.2:c.3632-26_3632-25insCGGGCTCTGCC XP_006710698.1:n.3632-26_3632-25insCGGGCTCTGCC
XM_011541429.1:c.3632-26_3632-25insCGGGCTCTGCC XP_011539731.1:n.3632-26_3632-25insCGGGCTCTGCC
XM_011541430.1:c.2759-26_2759-25insCGGGCTCTGCC XP_011539732.1:n.2759-26_2759-25insCGGGCTCTGCC
XM_011541431.1:c.1898-26_1898-25insCGGGCTCTGCC XP_011539733.1:n.1898-26_1898-25insCGGGCTCTGCC
XR_946650.1:n.3699-26_3699-25insCGGGCTCTGCC
NM_001364727.1:c.3317-26_3317-25insCGGGCTCTGCC NP_001351656.1:n.3317-26_3317-25insCGGGCTCTGCC
XM_005244749.3:c.3632-26_3632-25insCGGGCTCTGCC XP_005244806.1:n.3632-26_3632-25insCGGGCTCTGCC
XM_011541429.2:c.3632-26_3632-25insCGGGCTCTGCC XP_011539731.1:n.3632-26_3632-25insCGGGCTCTGCC
XR_946650.2:n.3703-26_3703-25insCGGGCTCTGCC
NM_001305275.2:c.3632-26_3632-25insCGGGCTCTGCC NP_001292204.1:n.3632-26_3632-25insCGGGCTCTGCC
NM_198576.4:c.3632-26_3632-25insCGGGCTCTGCC MANE Select NP_940978.2:n.3632-26_3632-25insCGGGCTCTGCC
NM_001364727.2:c.3317-26_3317-25insCGGGCTCTGCC NP_001351656.1:n.3317-26_3317-25insCGGGCTCTGCC