Canonical Allele Identifier: CA509745

Gene: AGRN

Linked Data

• dbSNP Id: rs772639284
• ExAC: 1:985591 G / GGC
• gnomAD v2: 1-985591-G-GGC
• gnomAD v4: 1-1050211-G-GGC
• MyVariant Identifiers: chr1:g.985591_985592insGC (hg19) ; chr1:g.1050211_1050212insGC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1050211_1050212insGC , CM000663.2:g.1050211_1050212insGC	GRCh38
NC_000001.10:g.985591_985592insGC , CM000663.1:g.985591_985592insGC	GRCh37
NC_000001.9:g.975454_975455insGC	NCBI36
NG_016346.1:g.35089_35090insGC , LRG_198:g.35089_35090insGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.4880-22_4880-21insGC MANE Select	ENSP00000368678.2:n.4880-22_4880-21insGC
ENST00000651234.1:c.4565-22_4565-21insGC	ENSP00000499046.1:n.4565-22_4565-21insGC
ENST00000652369.1:c.4565-22_4565-21insGC	ENSP00000498543.1:n.4565-22_4565-21insGC
ENST00000379370.6:c.4880-22_4880-21insGC	ENSP00000368678.2:n.4880-22_4880-21insGC
ENST00000620552.4:c.4466-22_4466-21insGC	ENSP00000484607.1:n.4466-22_4466-21insGC
NM_001305275.1:c.4880-22_4880-21insGC	NP_001292204.1:n.4880-22_4880-21insGC
NM_198576.3:c.4880-22_4880-21insGC	NP_940978.2:n.4880-22_4880-21insGC
XM_005244749.2:c.4880-22_4880-21insGC	XP_005244806.1:n.4880-22_4880-21insGC
XM_006710635.2:c.4880-22_4880-21insGC	XP_006710698.1:n.4880-22_4880-21insGC
XM_011541429.1:c.4880-22_4880-21insGC	XP_011539731.1:n.4880-22_4880-21insGC
XM_011541430.1:c.4007-22_4007-21insGC	XP_011539732.1:n.4007-22_4007-21insGC
XM_011541431.1:c.3146-22_3146-21insGC	XP_011539733.1:n.3146-22_3146-21insGC
XR_946650.1:n.4947-22_4947-21insGC
NM_001364727.1:c.4565-22_4565-21insGC	NP_001351656.1:n.4565-22_4565-21insGC
XM_005244749.3:c.4880-22_4880-21insGC	XP_005244806.1:n.4880-22_4880-21insGC
XM_011541429.2:c.4880-22_4880-21insGC	XP_011539731.1:n.4880-22_4880-21insGC
XR_946650.2:n.4951-22_4951-21insGC
NM_001305275.2:c.4880-22_4880-21insGC	NP_001292204.1:n.4880-22_4880-21insGC
NM_198576.4:c.4880-22_4880-21insGC MANE Select	NP_940978.2:n.4880-22_4880-21insGC
NM_001364727.2:c.4565-22_4565-21insGC	NP_001351656.1:n.4565-22_4565-21insGC