Canonical Allele Identifier: CA2574351304

Gene: AGRN

Linked Data

• gnomAD v4: 1-1043781-AGCCTGG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1043787_1043792del , CM000663.2:g.1043787_1043792del	GRCh38
NC_000001.10:g.979167_979172del , CM000663.1:g.979167_979172del	GRCh37
NC_000001.9:g.969030_969035del	NCBI36
NG_016346.1:g.28665_28670del , LRG_198:g.28665_28670del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.1799-36_1799-31del MANE Select	ENSP00000368678.2:n.1799-36_1799-31del
ENST00000651234.1:c.1484-36_1484-31del	ENSP00000499046.1:n.1484-36_1484-31del
ENST00000652369.1:c.1484-36_1484-31del	ENSP00000498543.1:n.1484-36_1484-31del
ENST00000379370.6:c.1799-36_1799-31del	ENSP00000368678.2:n.1799-36_1799-31del
ENST00000620552.4:c.1385-36_1385-31del	ENSP00000484607.1:n.1385-36_1385-31del
NM_001305275.1:c.1799-36_1799-31del	NP_001292204.1:n.1799-36_1799-31del
NM_198576.3:c.1799-36_1799-31del	NP_940978.2:n.1799-36_1799-31del
XM_005244749.2:c.1799-36_1799-31del	XP_005244806.1:n.1799-36_1799-31del
XM_006710635.2:c.1799-36_1799-31del	XP_006710698.1:n.1799-36_1799-31del
XM_011541429.1:c.1799-36_1799-31del	XP_011539731.1:n.1799-36_1799-31del
XM_011541430.1:c.926-36_926-31del	XP_011539732.1:n.926-36_926-31del
XM_011541431.1:c.65-36_65-31del	XP_011539733.1:n.65-36_65-31del
XR_946650.1:n.1866-36_1866-31del
NM_001364727.1:c.1484-36_1484-31del	NP_001351656.1:n.1484-36_1484-31del
XM_005244749.3:c.1799-36_1799-31del	XP_005244806.1:n.1799-36_1799-31del
XM_011541429.2:c.1799-36_1799-31del	XP_011539731.1:n.1799-36_1799-31del
XR_946650.2:n.1870-36_1870-31del
NM_001305275.2:c.1799-36_1799-31del	NP_001292204.1:n.1799-36_1799-31del
NM_198576.4:c.1799-36_1799-31del MANE Select	NP_940978.2:n.1799-36_1799-31del
NM_001364727.2:c.1484-36_1484-31del	NP_001351656.1:n.1484-36_1484-31del