Canonical Allele Identifier: CA884898928

Gene: AGRN

Linked Data

• dbSNP Id: rs1360724840
• gnomAD v3: 1-1049803-TG-T
• gnomAD v4: 1-1049803-TG-T
• MyVariant Identifiers: chr1:g.985184del (hg19) ; chr1:g.1049804del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1049807del , CM000663.2:g.1049807del	GRCh38
NC_000001.10:g.985187del , CM000663.1:g.985187del	GRCh37
NC_000001.9:g.975050del	NCBI36
NG_016346.1:g.34685del , LRG_198:g.34685del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.4744+12del MANE Select	ENSP00000368678.2:n.4744+12del
ENST00000651234.1:c.4429+12del	ENSP00000499046.1:n.4429+12del
ENST00000652369.1:c.4429+12del	ENSP00000498543.1:n.4429+12del
ENST00000379370.6:c.4744+12del	ENSP00000368678.2:n.4744+12del
ENST00000620552.4:c.4330+12del	ENSP00000484607.1:n.4330+12del
NM_001305275.1:c.4744+12del	NP_001292204.1:n.4744+12del
NM_198576.3:c.4744+12del	NP_940978.2:n.4744+12del
XM_005244749.2:c.4744+12del	XP_005244806.1:n.4744+12del
XM_006710635.2:c.4744+12del	XP_006710698.1:n.4744+12del
XM_011541429.1:c.4744+12del	XP_011539731.1:n.4744+12del
XM_011541430.1:c.3871+12del	XP_011539732.1:n.3871+12del
XM_011541431.1:c.3010+12del	XP_011539733.1:n.3010+12del
XR_946650.1:n.4811+12del
NM_001364727.1:c.4429+12del	NP_001351656.1:n.4429+12del
XM_005244749.3:c.4744+12del	XP_005244806.1:n.4744+12del
XM_011541429.2:c.4744+12del	XP_011539731.1:n.4744+12del
XR_946650.2:n.4815+12del
NM_001305275.2:c.4744+12del	NP_001292204.1:n.4744+12del
NM_198576.4:c.4744+12del MANE Select	NP_940978.2:n.4744+12del
NM_001364727.2:c.4429+12del	NP_001351656.1:n.4429+12del