Canonical Allele Identifier: CA1148771885

Gene: AGRN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1043807_1043809delinsGCT , CM000663.2:g.1043807_1043809delinsGCT	GRCh38
NC_000001.10:g.979187_979189delinsGCT , CM000663.1:g.979187_979189delinsGCT	GRCh37
NC_000001.9:g.969050_969052delinsGCT	NCBI36
NG_016346.1:g.28685_28687delinsGCT , LRG_198:g.28685_28687delinsGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.1799-16_1799-14delinsGCT MANE Select	ENSP00000368678.2:n.1799-16_1799-14delinsGCT
ENST00000651234.1:c.1484-16_1484-14delinsGCT	ENSP00000499046.1:n.1484-16_1484-14delinsGCT
ENST00000652369.1:c.1484-16_1484-14delinsGCT	ENSP00000498543.1:n.1484-16_1484-14delinsGCT
ENST00000379370.6:c.1799-16_1799-14delinsGCT	ENSP00000368678.2:n.1799-16_1799-14delinsGCT
ENST00000620552.4:c.1385-16_1385-14delinsGCT	ENSP00000484607.1:n.1385-16_1385-14delinsGCT
NM_001305275.1:c.1799-16_1799-14delinsGCT	NP_001292204.1:n.1799-16_1799-14delinsGCT
NM_198576.3:c.1799-16_1799-14delinsGCT	NP_940978.2:n.1799-16_1799-14delinsGCT
XM_005244749.2:c.1799-16_1799-14delinsGCT	XP_005244806.1:n.1799-16_1799-14delinsGCT
XM_006710635.2:c.1799-16_1799-14delinsGCT	XP_006710698.1:n.1799-16_1799-14delinsGCT
XM_011541429.1:c.1799-16_1799-14delinsGCT	XP_011539731.1:n.1799-16_1799-14delinsGCT
XM_011541430.1:c.926-16_926-14delinsGCT	XP_011539732.1:n.926-16_926-14delinsGCT
XM_011541431.1:c.65-16_65-14delinsGCT	XP_011539733.1:n.65-16_65-14delinsGCT
XR_946650.1:n.1866-16_1866-14delinsGCT
NM_001364727.1:c.1484-16_1484-14delinsGCT	NP_001351656.1:n.1484-16_1484-14delinsGCT
XM_005244749.3:c.1799-16_1799-14delinsGCT	XP_005244806.1:n.1799-16_1799-14delinsGCT
XM_011541429.2:c.1799-16_1799-14delinsGCT	XP_011539731.1:n.1799-16_1799-14delinsGCT
XR_946650.2:n.1870-16_1870-14delinsGCT
NM_001305275.2:c.1799-16_1799-14delinsGCT	NP_001292204.1:n.1799-16_1799-14delinsGCT
NM_198576.4:c.1799-16_1799-14delinsGCT MANE Select	NP_940978.2:n.1799-16_1799-14delinsGCT
NM_001364727.2:c.1484-16_1484-14delinsGCT	NP_001351656.1:n.1484-16_1484-14delinsGCT