Canonical Allele Identifier: CA1148748123

Gene: AGRN

Linked Data

• dbSNP Id: rs1645232273

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1050039_1050073del , CM000663.2:g.1050039_1050073del	GRCh38
NC_000001.10:g.985419_985453del , CM000663.1:g.985419_985453del	GRCh37
NC_000001.9:g.975282_975316del	NCBI36
NG_016346.1:g.34917_34951del , LRG_198:g.34917_34951del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.4879+2_4879+36del
ENST00000651234.1:c.4564+2_4564+36del
ENST00000652369.1:c.4564+2_4564+36del
ENST00000379370.6:c.4879+2_4879+36del
ENST00000620552.4:c.4465+2_4465+36del
NM_001305275.1:c.4879+2_4879+36del
NM_198576.3:c.4879+2_4879+36del
XM_005244749.2:c.4879+2_4879+36del
XM_006710635.2:c.4879+2_4879+36del
XM_011541429.1:c.4879+2_4879+36del
XM_011541430.1:c.4006+2_4006+36del
XM_011541431.1:c.3145+2_3145+36del
XR_946650.1:n.4946+2_4946+36del
NM_001364727.1:c.4564+2_4564+36del
XM_005244749.3:c.4879+2_4879+36del
XM_011541429.2:c.4879+2_4879+36del
XR_946650.2:n.4950+2_4950+36del
NM_001305275.2:c.4879+2_4879+36del
NM_198576.4:c.4879+2_4879+36del
NM_001364727.2:c.4564+2_4564+36del