Canonical Allele Identifier: CA509693

Gene: AGRN

Linked Data

• dbSNP Id: rs773658650
• ExAC: 1:985442 CAG / C
• gnomAD v2: 1-985442-CAG-C
• gnomAD v3: 1-1050062-CAG-C
• gnomAD v4: 1-1050062-CAG-C
• MyVariant Identifiers: chr1:g.985443_985444del (hg19) ; chr1:g.985443_985445delinsG (hg19) ; chr1:g.985443_985446delinsGG (hg19) ; chr1:g.1050063_1050064del (hg38) ; chr1:g.1050063_1050065delinsG (hg38) ; chr1:g.1050063_1050066delinsGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1050063_1050064del , CM000663.2:g.1050063_1050064del	GRCh38
NC_000001.10:g.985443_985444del , CM000663.1:g.985443_985444del	GRCh37
NC_000001.9:g.975306_975307del	NCBI36
NG_016346.1:g.34941_34942del , LRG_198:g.34941_34942del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.4879+26_4879+27del MANE Select	ENSP00000368678.2:n.4879+26_4879+27del
ENST00000651234.1:c.4564+26_4564+27del	ENSP00000499046.1:n.4564+26_4564+27del
ENST00000652369.1:c.4564+26_4564+27del	ENSP00000498543.1:n.4564+26_4564+27del
ENST00000379370.6:c.4879+26_4879+27del	ENSP00000368678.2:n.4879+26_4879+27del
ENST00000620552.4:c.4465+26_4465+27del	ENSP00000484607.1:n.4465+26_4465+27del
NM_001305275.1:c.4879+26_4879+27del	NP_001292204.1:n.4879+26_4879+27del
NM_198576.3:c.4879+26_4879+27del	NP_940978.2:n.4879+26_4879+27del
XM_005244749.2:c.4879+26_4879+27del	XP_005244806.1:n.4879+26_4879+27del
XM_006710635.2:c.4879+26_4879+27del	XP_006710698.1:n.4879+26_4879+27del
XM_011541429.1:c.4879+26_4879+27del	XP_011539731.1:n.4879+26_4879+27del
XM_011541430.1:c.4006+26_4006+27del	XP_011539732.1:n.4006+26_4006+27del
XM_011541431.1:c.3145+26_3145+27del	XP_011539733.1:n.3145+26_3145+27del
XR_946650.1:n.4946+26_4946+27del
NM_001364727.1:c.4564+26_4564+27del	NP_001351656.1:n.4564+26_4564+27del
XM_005244749.3:c.4879+26_4879+27del	XP_005244806.1:n.4879+26_4879+27del
XM_011541429.2:c.4879+26_4879+27del	XP_011539731.1:n.4879+26_4879+27del
XR_946650.2:n.4950+26_4950+27del
NM_001305275.2:c.4879+26_4879+27del	NP_001292204.1:n.4879+26_4879+27del
NM_198576.4:c.4879+26_4879+27del MANE Select	NP_940978.2:n.4879+26_4879+27del
NM_001364727.2:c.4564+26_4564+27del	NP_001351656.1:n.4564+26_4564+27del