Canonical Allele Identifier: CA884897865

Gene: AGRN

Linked Data

• dbSNP Id: rs1415643475
• gnomAD v4: 1-1047928-G-GC
• MyVariant Identifiers: chr1:g.983308_983309insC (hg19) ; chr1:g.1047928_1047929insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1047933dup , CM000663.2:g.1047933dup	GRCh38
NC_000001.10:g.983313dup , CM000663.1:g.983313dup	GRCh37
NC_000001.9:g.973176dup	NCBI36
NG_016346.1:g.32811dup , LRG_198:g.32811dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.3751+38dup MANE Select	ENSP00000368678.2:n.3751+38dup
ENST00000651234.1:c.3436+38dup	ENSP00000499046.1:n.3436+38dup
ENST00000652369.1:c.3436+38dup	ENSP00000498543.1:n.3436+38dup
ENST00000379370.6:c.3751+38dup	ENSP00000368678.2:n.3751+38dup
ENST00000620552.4:c.3337+38dup	ENSP00000484607.1:n.3337+38dup
NM_001305275.1:c.3751+38dup	NP_001292204.1:n.3751+38dup
NM_198576.3:c.3751+38dup	NP_940978.2:n.3751+38dup
XM_005244749.2:c.3751+38dup	XP_005244806.1:n.3751+38dup
XM_006710635.2:c.3751+38dup	XP_006710698.1:n.3751+38dup
XM_011541429.1:c.3751+38dup	XP_011539731.1:n.3751+38dup
XM_011541430.1:c.2878+38dup	XP_011539732.1:n.2878+38dup
XM_011541431.1:c.2017+38dup	XP_011539733.1:n.2017+38dup
XR_946650.1:n.3818+38dup
NM_001364727.1:c.3436+38dup	NP_001351656.1:n.3436+38dup
XM_005244749.3:c.3751+38dup	XP_005244806.1:n.3751+38dup
XM_011541429.2:c.3751+38dup	XP_011539731.1:n.3751+38dup
XR_946650.2:n.3822+38dup
NM_001305275.2:c.3751+38dup	NP_001292204.1:n.3751+38dup
NM_198576.4:c.3751+38dup MANE Select	NP_940978.2:n.3751+38dup
NM_001364727.2:c.3436+38dup	NP_001351656.1:n.3436+38dup