Canonical Allele Identifier: CA884897878

Gene: AGRN

Linked Data

• dbSNP Id: rs1201054826
• MyVariant Identifiers: chr1:g.983339_983340insC (hg19) ; chr1:g.1047959_1047960insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1047963dup , CM000663.2:g.1047963dup	GRCh38
NC_000001.10:g.983343dup , CM000663.1:g.983343dup	GRCh37
NC_000001.9:g.973206dup	NCBI36
NG_016346.1:g.32841dup , LRG_198:g.32841dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.3752-49dup MANE Select	ENSP00000368678.2:n.3752-49dup
ENST00000651234.1:c.3437-49dup	ENSP00000499046.1:n.3437-49dup
ENST00000652369.1:c.3437-49dup	ENSP00000498543.1:n.3437-49dup
ENST00000379370.6:c.3752-49dup	ENSP00000368678.2:n.3752-49dup
ENST00000620552.4:c.3338-49dup	ENSP00000484607.1:n.3338-49dup
NM_001305275.1:c.3752-49dup	NP_001292204.1:n.3752-49dup
NM_198576.3:c.3752-49dup	NP_940978.2:n.3752-49dup
XM_005244749.2:c.3752-49dup	XP_005244806.1:n.3752-49dup
XM_006710635.2:c.3752-49dup	XP_006710698.1:n.3752-49dup
XM_011541429.1:c.3752-49dup	XP_011539731.1:n.3752-49dup
XM_011541430.1:c.2879-49dup	XP_011539732.1:n.2879-49dup
XM_011541431.1:c.2018-49dup	XP_011539733.1:n.2018-49dup
XR_946650.1:n.3819-49dup
NM_001364727.1:c.3437-49dup	NP_001351656.1:n.3437-49dup
XM_005244749.3:c.3752-49dup	XP_005244806.1:n.3752-49dup
XM_011541429.2:c.3752-49dup	XP_011539731.1:n.3752-49dup
XR_946650.2:n.3823-49dup
NM_001305275.2:c.3752-49dup	NP_001292204.1:n.3752-49dup
NM_198576.4:c.3752-49dup MANE Select	NP_940978.2:n.3752-49dup
NM_001364727.2:c.3437-49dup	NP_001351656.1:n.3437-49dup