Canonical Allele Identifier: CA884897557

Gene: AGRN

Linked Data

• dbSNP Id: rs1182417747
• gnomAD v4: 1-1047707-C-CCCTT
• MyVariant Identifiers: chr1:g.983087_983088insCCTT (hg19) ; chr1:g.1047707_1047708insCCTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1047711_1047714dup , CM000663.2:g.1047711_1047714dup	GRCh38
NC_000001.10:g.983091_983094dup , CM000663.1:g.983091_983094dup	GRCh37
NC_000001.9:g.972954_972957dup	NCBI36
NG_016346.1:g.32589_32592dup , LRG_198:g.32589_32592dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.3631+24_3631+27dup MANE Select	ENSP00000368678.2:n.3631+24_3631+27dup
ENST00000651234.1:c.3316+24_3316+27dup	ENSP00000499046.1:n.3316+24_3316+27dup
ENST00000652369.1:c.3316+24_3316+27dup	ENSP00000498543.1:n.3316+24_3316+27dup
ENST00000379370.6:c.3631+24_3631+27dup	ENSP00000368678.2:n.3631+24_3631+27dup
ENST00000466223.1:n.369+24_369+27dup
ENST00000478677.1:n.213+24_213+27dup
ENST00000620552.4:c.3217+24_3217+27dup	ENSP00000484607.1:n.3217+24_3217+27dup
NM_001305275.1:c.3631+24_3631+27dup	NP_001292204.1:n.3631+24_3631+27dup
NM_198576.3:c.3631+24_3631+27dup	NP_940978.2:n.3631+24_3631+27dup
XM_005244749.2:c.3631+24_3631+27dup	XP_005244806.1:n.3631+24_3631+27dup
XM_006710635.2:c.3631+24_3631+27dup	XP_006710698.1:n.3631+24_3631+27dup
XM_011541429.1:c.3631+24_3631+27dup	XP_011539731.1:n.3631+24_3631+27dup
XM_011541430.1:c.2758+24_2758+27dup	XP_011539732.1:n.2758+24_2758+27dup
XM_011541431.1:c.1897+24_1897+27dup	XP_011539733.1:n.1897+24_1897+27dup
XR_946650.1:n.3698+24_3698+27dup
NM_001364727.1:c.3316+24_3316+27dup	NP_001351656.1:n.3316+24_3316+27dup
XM_005244749.3:c.3631+24_3631+27dup	XP_005244806.1:n.3631+24_3631+27dup
XM_011541429.2:c.3631+24_3631+27dup	XP_011539731.1:n.3631+24_3631+27dup
XR_946650.2:n.3702+24_3702+27dup
NM_001305275.2:c.3631+24_3631+27dup	NP_001292204.1:n.3631+24_3631+27dup
NM_198576.4:c.3631+24_3631+27dup MANE Select	NP_940978.2:n.3631+24_3631+27dup
NM_001364727.2:c.3316+24_3316+27dup	NP_001351656.1:n.3316+24_3316+27dup