Canonical Allele Identifier: CA2642491992
Gene: AGRN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1047952_1047957del , CM000663.2:g.1047952_1047957del GRCh38
NC_000001.10:g.983332_983337del , CM000663.1:g.983332_983337del GRCh37
NC_000001.9:g.973195_973200del NCBI36
NG_016346.1:g.32830_32835del , LRG_198:g.32830_32835del

Transcript Alleles

HGVS Amino-acid Change
ENST00000379370.7:c.3751+57_3752-55del MANE Select ENSP00000368678.2:n.3751+57_3752-55del
ENST00000651234.1:c.3436+57_3437-55del ENSP00000499046.1:n.3436+57_3437-55del
ENST00000652369.1:c.3436+57_3437-55del ENSP00000498543.1:n.3436+57_3437-55del
ENST00000379370.6:c.3751+57_3752-55del ENSP00000368678.2:n.3751+57_3752-55del
ENST00000620552.4:c.3337+57_3338-55del ENSP00000484607.1:n.3337+57_3338-55del
NM_001305275.1:c.3751+57_3752-55del NP_001292204.1:n.3751+57_3752-55del
NM_198576.3:c.3751+57_3752-55del NP_940978.2:n.3751+57_3752-55del
XM_005244749.2:c.3751+57_3752-55del XP_005244806.1:n.3751+57_3752-55del
XM_006710635.2:c.3751+57_3752-55del XP_006710698.1:n.3751+57_3752-55del
XM_011541429.1:c.3751+57_3752-55del XP_011539731.1:n.3751+57_3752-55del
XM_011541430.1:c.2878+57_2879-55del XP_011539732.1:n.2878+57_2879-55del
XM_011541431.1:c.2017+57_2018-55del XP_011539733.1:n.2017+57_2018-55del
XR_946650.1:n.3818+57_3819-55del
NM_001364727.1:c.3436+57_3437-55del NP_001351656.1:n.3436+57_3437-55del
XM_005244749.3:c.3751+57_3752-55del XP_005244806.1:n.3751+57_3752-55del
XM_011541429.2:c.3751+57_3752-55del XP_011539731.1:n.3751+57_3752-55del
XR_946650.2:n.3822+57_3823-55del
NM_001305275.2:c.3751+57_3752-55del NP_001292204.1:n.3751+57_3752-55del
NM_198576.4:c.3751+57_3752-55del MANE Select NP_940978.2:n.3751+57_3752-55del
NM_001364727.2:c.3436+57_3437-55del NP_001351656.1:n.3436+57_3437-55del