Canonical Allele Identifier: CA1148771681

Gene: AGRN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1043788_1043789delinsGC , CM000663.2:g.1043788_1043789delinsGC	GRCh38
NC_000001.10:g.979168_979169delinsGC , CM000663.1:g.979168_979169delinsGC	GRCh37
NC_000001.9:g.969031_969032delinsGC	NCBI36
NG_016346.1:g.28666_28667delinsGC , LRG_198:g.28666_28667delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.1799-35_1799-34delinsGC MANE Select	ENSP00000368678.2:n.1799-35_1799-34delinsGC
ENST00000651234.1:c.1484-35_1484-34delinsGC	ENSP00000499046.1:n.1484-35_1484-34delinsGC
ENST00000652369.1:c.1484-35_1484-34delinsGC	ENSP00000498543.1:n.1484-35_1484-34delinsGC
ENST00000379370.6:c.1799-35_1799-34delinsGC	ENSP00000368678.2:n.1799-35_1799-34delinsGC
ENST00000620552.4:c.1385-35_1385-34delinsGC	ENSP00000484607.1:n.1385-35_1385-34delinsGC
NM_001305275.1:c.1799-35_1799-34delinsGC	NP_001292204.1:n.1799-35_1799-34delinsGC
NM_198576.3:c.1799-35_1799-34delinsGC	NP_940978.2:n.1799-35_1799-34delinsGC
XM_005244749.2:c.1799-35_1799-34delinsGC	XP_005244806.1:n.1799-35_1799-34delinsGC
XM_006710635.2:c.1799-35_1799-34delinsGC	XP_006710698.1:n.1799-35_1799-34delinsGC
XM_011541429.1:c.1799-35_1799-34delinsGC	XP_011539731.1:n.1799-35_1799-34delinsGC
XM_011541430.1:c.926-35_926-34delinsGC	XP_011539732.1:n.926-35_926-34delinsGC
XM_011541431.1:c.65-35_65-34delinsGC	XP_011539733.1:n.65-35_65-34delinsGC
XR_946650.1:n.1866-35_1866-34delinsGC
NM_001364727.1:c.1484-35_1484-34delinsGC	NP_001351656.1:n.1484-35_1484-34delinsGC
XM_005244749.3:c.1799-35_1799-34delinsGC	XP_005244806.1:n.1799-35_1799-34delinsGC
XM_011541429.2:c.1799-35_1799-34delinsGC	XP_011539731.1:n.1799-35_1799-34delinsGC
XR_946650.2:n.1870-35_1870-34delinsGC
NM_001305275.2:c.1799-35_1799-34delinsGC	NP_001292204.1:n.1799-35_1799-34delinsGC
NM_198576.4:c.1799-35_1799-34delinsGC MANE Select	NP_940978.2:n.1799-35_1799-34delinsGC
NM_001364727.2:c.1484-35_1484-34delinsGC	NP_001351656.1:n.1484-35_1484-34delinsGC