Canonical Allele Identifier: CA509747

Gene: AGRN

Linked Data

• dbSNP Id: rs773533692
• ExAC: 1:985600 ACT / A
• gnomAD v2: 1-985600-ACT-A
• gnomAD v3: 1-1050220-ACT-A
• gnomAD v4: 1-1050220-ACT-A
• MyVariant Identifiers: chr1:g.985601_985602del (hg19) ; chr1:g.1050221_1050222del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1050224_1050225del , CM000663.2:g.1050224_1050225del	GRCh38
NC_000001.10:g.985604_985605del , CM000663.1:g.985604_985605del	GRCh37
NC_000001.9:g.975467_975468del	NCBI36
NG_016346.1:g.35102_35103del , LRG_198:g.35102_35103del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.4880-9_4880-8del MANE Select	ENSP00000368678.2:n.4880-9_4880-8del
ENST00000651234.1:c.4565-9_4565-8del	ENSP00000499046.1:n.4565-9_4565-8del
ENST00000652369.1:c.4565-9_4565-8del	ENSP00000498543.1:n.4565-9_4565-8del
ENST00000379370.6:c.4880-9_4880-8del	ENSP00000368678.2:n.4880-9_4880-8del
ENST00000620552.4:c.4466-9_4466-8del	ENSP00000484607.1:n.4466-9_4466-8del
NM_001305275.1:c.4880-9_4880-8del	NP_001292204.1:n.4880-9_4880-8del
NM_198576.3:c.4880-9_4880-8del	NP_940978.2:n.4880-9_4880-8del
XM_005244749.2:c.4880-9_4880-8del	XP_005244806.1:n.4880-9_4880-8del
XM_006710635.2:c.4880-9_4880-8del	XP_006710698.1:n.4880-9_4880-8del
XM_011541429.1:c.4880-9_4880-8del	XP_011539731.1:n.4880-9_4880-8del
XM_011541430.1:c.4007-9_4007-8del	XP_011539732.1:n.4007-9_4007-8del
XM_011541431.1:c.3146-9_3146-8del	XP_011539733.1:n.3146-9_3146-8del
XR_946650.1:n.4947-9_4947-8del
NM_001364727.1:c.4565-9_4565-8del	NP_001351656.1:n.4565-9_4565-8del
XM_005244749.3:c.4880-9_4880-8del	XP_005244806.1:n.4880-9_4880-8del
XM_011541429.2:c.4880-9_4880-8del	XP_011539731.1:n.4880-9_4880-8del
XR_946650.2:n.4951-9_4951-8del
NM_001305275.2:c.4880-9_4880-8del	NP_001292204.1:n.4880-9_4880-8del
NM_198576.4:c.4880-9_4880-8del MANE Select	NP_940978.2:n.4880-9_4880-8del
NM_001364727.2:c.4565-9_4565-8del	NP_001351656.1:n.4565-9_4565-8del