Canonical Allele Identifier: CA884897568

Gene: AGRN

Linked Data

• dbSNP Id: rs1356351416
• gnomAD v3: 1-1047728-T-TG
• gnomAD v4: 1-1047728-T-TG
• MyVariant Identifiers: chr1:g.983108_983109insG (hg19) ; chr1:g.1047728_1047729insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1047733dup , CM000663.2:g.1047733dup	GRCh38
NC_000001.10:g.983113dup , CM000663.1:g.983113dup	GRCh37
NC_000001.9:g.972976dup	NCBI36
NG_016346.1:g.32611dup , LRG_198:g.32611dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.3632-43dup MANE Select	ENSP00000368678.2:n.3632-43dup
ENST00000651234.1:c.3317-43dup	ENSP00000499046.1:n.3317-43dup
ENST00000652369.1:c.3317-43dup	ENSP00000498543.1:n.3317-43dup
ENST00000379370.6:c.3632-43dup	ENSP00000368678.2:n.3632-43dup
ENST00000466223.1:n.370-43dup
ENST00000478677.1:n.214-43dup
ENST00000620552.4:c.3218-43dup	ENSP00000484607.1:n.3218-43dup
NM_001305275.1:c.3632-43dup	NP_001292204.1:n.3632-43dup
NM_198576.3:c.3632-43dup	NP_940978.2:n.3632-43dup
XM_005244749.2:c.3632-43dup	XP_005244806.1:n.3632-43dup
XM_006710635.2:c.3632-43dup	XP_006710698.1:n.3632-43dup
XM_011541429.1:c.3632-43dup	XP_011539731.1:n.3632-43dup
XM_011541430.1:c.2759-43dup	XP_011539732.1:n.2759-43dup
XM_011541431.1:c.1898-43dup	XP_011539733.1:n.1898-43dup
XR_946650.1:n.3699-43dup
NM_001364727.1:c.3317-43dup	NP_001351656.1:n.3317-43dup
XM_005244749.3:c.3632-43dup	XP_005244806.1:n.3632-43dup
XM_011541429.2:c.3632-43dup	XP_011539731.1:n.3632-43dup
XR_946650.2:n.3703-43dup
NM_001305275.2:c.3632-43dup	NP_001292204.1:n.3632-43dup
NM_198576.4:c.3632-43dup MANE Select	NP_940978.2:n.3632-43dup
NM_001364727.2:c.3317-43dup	NP_001351656.1:n.3317-43dup