Canonical Allele Identifier: CA1148749450

Gene: AGRN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1050190_1050191delinsGC , CM000663.2:g.1050190_1050191delinsGC	GRCh38
NC_000001.10:g.985570_985571delinsGC , CM000663.1:g.985570_985571delinsGC	GRCh37
NC_000001.9:g.975433_975434delinsGC	NCBI36
NG_016346.1:g.35068_35069delinsGC , LRG_198:g.35068_35069delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.4880-43_4880-42delinsGC MANE Select	ENSP00000368678.2:n.4880-43_4880-42delinsGC
ENST00000651234.1:c.4565-43_4565-42delinsGC	ENSP00000499046.1:n.4565-43_4565-42delinsGC
ENST00000652369.1:c.4565-43_4565-42delinsGC	ENSP00000498543.1:n.4565-43_4565-42delinsGC
ENST00000379370.6:c.4880-43_4880-42delinsGC	ENSP00000368678.2:n.4880-43_4880-42delinsGC
ENST00000620552.4:c.4466-43_4466-42delinsGC	ENSP00000484607.1:n.4466-43_4466-42delinsGC
NM_001305275.1:c.4880-43_4880-42delinsGC	NP_001292204.1:n.4880-43_4880-42delinsGC
NM_198576.3:c.4880-43_4880-42delinsGC	NP_940978.2:n.4880-43_4880-42delinsGC
XM_005244749.2:c.4880-43_4880-42delinsGC	XP_005244806.1:n.4880-43_4880-42delinsGC
XM_006710635.2:c.4880-43_4880-42delinsGC	XP_006710698.1:n.4880-43_4880-42delinsGC
XM_011541429.1:c.4880-43_4880-42delinsGC	XP_011539731.1:n.4880-43_4880-42delinsGC
XM_011541430.1:c.4007-43_4007-42delinsGC	XP_011539732.1:n.4007-43_4007-42delinsGC
XM_011541431.1:c.3146-43_3146-42delinsGC	XP_011539733.1:n.3146-43_3146-42delinsGC
XR_946650.1:n.4947-43_4947-42delinsGC
NM_001364727.1:c.4565-43_4565-42delinsGC	NP_001351656.1:n.4565-43_4565-42delinsGC
XM_005244749.3:c.4880-43_4880-42delinsGC	XP_005244806.1:n.4880-43_4880-42delinsGC
XM_011541429.2:c.4880-43_4880-42delinsGC	XP_011539731.1:n.4880-43_4880-42delinsGC
XR_946650.2:n.4951-43_4951-42delinsGC
NM_001305275.2:c.4880-43_4880-42delinsGC	NP_001292204.1:n.4880-43_4880-42delinsGC
NM_198576.4:c.4880-43_4880-42delinsGC MANE Select	NP_940978.2:n.4880-43_4880-42delinsGC
NM_001364727.2:c.4565-43_4565-42delinsGC	NP_001351656.1:n.4565-43_4565-42delinsGC