Canonical Allele Identifier: CA1148749192

Gene: AGRN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1050133_1050138delinsCAGTCT , CM000663.2:g.1050133_1050138delinsCAGTCT	GRCh38
NC_000001.10:g.985513_985518delinsCAGTCT , CM000663.1:g.985513_985518delinsCAGTCT	GRCh37
NC_000001.9:g.975376_975381delinsCAGTCT	NCBI36
NG_016346.1:g.35011_35016delinsCAGTCT , LRG_198:g.35011_35016delinsCAGTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.4879+96_4880-95delinsCAGTCT MANE Select	ENSP00000368678.2:n.4879+96_4880-95delinsCAGTCT
ENST00000651234.1:c.4564+96_4565-95delinsCAGTCT	ENSP00000499046.1:n.4564+96_4565-95delinsCAGTCT
ENST00000652369.1:c.4564+96_4565-95delinsCAGTCT	ENSP00000498543.1:n.4564+96_4565-95delinsCAGTCT
ENST00000379370.6:c.4879+96_4880-95delinsCAGTCT	ENSP00000368678.2:n.4879+96_4880-95delinsCAGTCT
ENST00000620552.4:c.4465+96_4466-95delinsCAGTCT	ENSP00000484607.1:n.4465+96_4466-95delinsCAGTCT
NM_001305275.1:c.4879+96_4880-95delinsCAGTCT	NP_001292204.1:n.4879+96_4880-95delinsCAGTCT
NM_198576.3:c.4879+96_4880-95delinsCAGTCT	NP_940978.2:n.4879+96_4880-95delinsCAGTCT
XM_005244749.2:c.4879+96_4880-95delinsCAGTCT	XP_005244806.1:n.4879+96_4880-95delinsCAGTCT
XM_006710635.2:c.4879+96_4880-95delinsCAGTCT	XP_006710698.1:n.4879+96_4880-95delinsCAGTCT
XM_011541429.1:c.4879+96_4880-95delinsCAGTCT	XP_011539731.1:n.4879+96_4880-95delinsCAGTCT
XM_011541430.1:c.4006+96_4007-95delinsCAGTCT	XP_011539732.1:n.4006+96_4007-95delinsCAGTCT
XM_011541431.1:c.3145+96_3146-95delinsCAGTCT	XP_011539733.1:n.3145+96_3146-95delinsCAGTCT
XR_946650.1:n.4946+96_4947-95delinsCAGTCT
NM_001364727.1:c.4564+96_4565-95delinsCAGTCT	NP_001351656.1:n.4564+96_4565-95delinsCAGTCT
XM_005244749.3:c.4879+96_4880-95delinsCAGTCT	XP_005244806.1:n.4879+96_4880-95delinsCAGTCT
XM_011541429.2:c.4879+96_4880-95delinsCAGTCT	XP_011539731.1:n.4879+96_4880-95delinsCAGTCT
XR_946650.2:n.4950+96_4951-95delinsCAGTCT
NM_001305275.2:c.4879+96_4880-95delinsCAGTCT	NP_001292204.1:n.4879+96_4880-95delinsCAGTCT
NM_198576.4:c.4879+96_4880-95delinsCAGTCT MANE Select	NP_940978.2:n.4879+96_4880-95delinsCAGTCT
NM_001364727.2:c.4564+96_4565-95delinsCAGTCT	NP_001351656.1:n.4564+96_4565-95delinsCAGTCT