Canonical Allele Identifier: CA1148771839

Gene: AGRN

Linked Data

• dbSNP Id: rs1645014267

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1043803_1043806del , CM000663.2:g.1043803_1043806del	GRCh38
NC_000001.10:g.979183_979186del , CM000663.1:g.979183_979186del	GRCh37
NC_000001.9:g.969046_969049del	NCBI36
NG_016346.1:g.28681_28684del , LRG_198:g.28681_28684del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.1799-20_1799-17del MANE Select	ENSP00000368678.2:n.1799-20_1799-17del
ENST00000651234.1:c.1484-20_1484-17del	ENSP00000499046.1:n.1484-20_1484-17del
ENST00000652369.1:c.1484-20_1484-17del	ENSP00000498543.1:n.1484-20_1484-17del
ENST00000379370.6:c.1799-20_1799-17del	ENSP00000368678.2:n.1799-20_1799-17del
ENST00000620552.4:c.1385-20_1385-17del	ENSP00000484607.1:n.1385-20_1385-17del
NM_001305275.1:c.1799-20_1799-17del	NP_001292204.1:n.1799-20_1799-17del
NM_198576.3:c.1799-20_1799-17del	NP_940978.2:n.1799-20_1799-17del
XM_005244749.2:c.1799-20_1799-17del	XP_005244806.1:n.1799-20_1799-17del
XM_006710635.2:c.1799-20_1799-17del	XP_006710698.1:n.1799-20_1799-17del
XM_011541429.1:c.1799-20_1799-17del	XP_011539731.1:n.1799-20_1799-17del
XM_011541430.1:c.926-20_926-17del	XP_011539732.1:n.926-20_926-17del
XM_011541431.1:c.65-20_65-17del	XP_011539733.1:n.65-20_65-17del
XR_946650.1:n.1866-20_1866-17del
NM_001364727.1:c.1484-20_1484-17del	NP_001351656.1:n.1484-20_1484-17del
XM_005244749.3:c.1799-20_1799-17del	XP_005244806.1:n.1799-20_1799-17del
XM_011541429.2:c.1799-20_1799-17del	XP_011539731.1:n.1799-20_1799-17del
XR_946650.2:n.1870-20_1870-17del
NM_001305275.2:c.1799-20_1799-17del	NP_001292204.1:n.1799-20_1799-17del
NM_198576.4:c.1799-20_1799-17del MANE Select	NP_940978.2:n.1799-20_1799-17del
NM_001364727.2:c.1484-20_1484-17del	NP_001351656.1:n.1484-20_1484-17del