Canonical Allele Identifier: CA520619328

Gene: AGRN

Linked Data

• dbSNP Id: rs1557718193
• gnomAD v2: 1-985174-C-CGGTGAGGGTGGGGCCGGGGCG
• gnomAD v4: 1-1049794-C-CGGTGAGGGTGGGGCCGGGGCG
• MyVariant Identifiers: chr1:g.985174_985175insGGTGAGGGTGGGGCCGGGGCG (hg19) ; chr1:g.1049794_1049795insGGTGAGGGTGGGGCCGGGGCG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1049799_1049819dup , CM000663.2:g.1049799_1049819dup	GRCh38
NC_000001.10:g.985179_985199dup , CM000663.1:g.985179_985199dup	GRCh37
NC_000001.9:g.975042_975062dup	NCBI36
NG_016346.1:g.34677_34697dup , LRG_198:g.34677_34697dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.4744+4_4744+24dup
ENST00000651234.1:c.4429+4_4429+24dup
ENST00000652369.1:c.4429+4_4429+24dup
ENST00000379370.6:c.4744+4_4744+24dup
ENST00000620552.4:c.4330+4_4330+24dup
NM_001305275.1:c.4744+4_4744+24dup
NM_198576.3:c.4744+4_4744+24dup
XM_005244749.2:c.4744+4_4744+24dup
XM_006710635.2:c.4744+4_4744+24dup
XM_011541429.1:c.4744+4_4744+24dup
XM_011541430.1:c.3871+4_3871+24dup
XM_011541431.1:c.3010+4_3010+24dup
XR_946650.1:n.4811+4_4811+24dup
NM_001364727.1:c.4429+4_4429+24dup
XM_005244749.3:c.4744+4_4744+24dup
XM_011541429.2:c.4744+4_4744+24dup
XR_946650.2:n.4815+4_4815+24dup
NM_001305275.2:c.4744+4_4744+24dup
NM_198576.4:c.4744+4_4744+24dup
NM_001364727.2:c.4429+4_4429+24dup