Canonical Allele Identifier: CA884820064

Gene: AGRN

Linked Data

• dbSNP Id: rs1166550650
• gnomAD v3: 1-1043807-GCT-G
• gnomAD v4: 1-1043807-GCT-G
• MyVariant Identifiers: chr1:g.979188_979189del (hg19) ; chr1:g.1043808_1043809del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1043810_1043811del , CM000663.2:g.1043810_1043811del	GRCh38
NC_000001.10:g.979190_979191del , CM000663.1:g.979190_979191del	GRCh37
NC_000001.9:g.969053_969054del	NCBI36
NG_016346.1:g.28688_28689del , LRG_198:g.28688_28689del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.1799-13_1799-12del MANE Select	ENSP00000368678.2:n.1799-13_1799-12del
ENST00000651234.1:c.1484-13_1484-12del	ENSP00000499046.1:n.1484-13_1484-12del
ENST00000652369.1:c.1484-13_1484-12del	ENSP00000498543.1:n.1484-13_1484-12del
ENST00000379370.6:c.1799-13_1799-12del	ENSP00000368678.2:n.1799-13_1799-12del
ENST00000620552.4:c.1385-13_1385-12del	ENSP00000484607.1:n.1385-13_1385-12del
NM_001305275.1:c.1799-13_1799-12del	NP_001292204.1:n.1799-13_1799-12del
NM_198576.3:c.1799-13_1799-12del	NP_940978.2:n.1799-13_1799-12del
XM_005244749.2:c.1799-13_1799-12del	XP_005244806.1:n.1799-13_1799-12del
XM_006710635.2:c.1799-13_1799-12del	XP_006710698.1:n.1799-13_1799-12del
XM_011541429.1:c.1799-13_1799-12del	XP_011539731.1:n.1799-13_1799-12del
XM_011541430.1:c.926-13_926-12del	XP_011539732.1:n.926-13_926-12del
XM_011541431.1:c.65-13_65-12del	XP_011539733.1:n.65-13_65-12del
XR_946650.1:n.1866-13_1866-12del
NM_001364727.1:c.1484-13_1484-12del	NP_001351656.1:n.1484-13_1484-12del
XM_005244749.3:c.1799-13_1799-12del	XP_005244806.1:n.1799-13_1799-12del
XM_011541429.2:c.1799-13_1799-12del	XP_011539731.1:n.1799-13_1799-12del
XR_946650.2:n.1870-13_1870-12del
NM_001305275.2:c.1799-13_1799-12del	NP_001292204.1:n.1799-13_1799-12del
NM_198576.4:c.1799-13_1799-12del MANE Select	NP_940978.2:n.1799-13_1799-12del
NM_001364727.2:c.1484-13_1484-12del	NP_001351656.1:n.1484-13_1484-12del