Canonical Allele Identifier: CA1148748485

Gene: AGRN

Linked Data

• dbSNP Id: rs1645234921

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1050066_1050069delinsTGGA , CM000663.2:g.1050066_1050069delinsTGGA	GRCh38
NC_000001.10:g.985446_985449delinsTGGA , CM000663.1:g.985446_985449delinsTGGA	GRCh37
NC_000001.9:g.975309_975312delinsTGGA	NCBI36
NG_016346.1:g.34944_34947delinsTGGA , LRG_198:g.34944_34947delinsTGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.4879+29_4879+32delinsTGGA MANE Select	ENSP00000368678.2:n.4879+29_4879+32delinsTGGA
ENST00000651234.1:c.4564+29_4564+32delinsTGGA	ENSP00000499046.1:n.4564+29_4564+32delinsTGGA
ENST00000652369.1:c.4564+29_4564+32delinsTGGA	ENSP00000498543.1:n.4564+29_4564+32delinsTGGA
ENST00000379370.6:c.4879+29_4879+32delinsTGGA	ENSP00000368678.2:n.4879+29_4879+32delinsTGGA
ENST00000620552.4:c.4465+29_4465+32delinsTGGA	ENSP00000484607.1:n.4465+29_4465+32delinsTGGA
NM_001305275.1:c.4879+29_4879+32delinsTGGA	NP_001292204.1:n.4879+29_4879+32delinsTGGA
NM_198576.3:c.4879+29_4879+32delinsTGGA	NP_940978.2:n.4879+29_4879+32delinsTGGA
XM_005244749.2:c.4879+29_4879+32delinsTGGA	XP_005244806.1:n.4879+29_4879+32delinsTGGA
XM_006710635.2:c.4879+29_4879+32delinsTGGA	XP_006710698.1:n.4879+29_4879+32delinsTGGA
XM_011541429.1:c.4879+29_4879+32delinsTGGA	XP_011539731.1:n.4879+29_4879+32delinsTGGA
XM_011541430.1:c.4006+29_4006+32delinsTGGA	XP_011539732.1:n.4006+29_4006+32delinsTGGA
XM_011541431.1:c.3145+29_3145+32delinsTGGA	XP_011539733.1:n.3145+29_3145+32delinsTGGA
XR_946650.1:n.4946+29_4946+32delinsTGGA
NM_001364727.1:c.4564+29_4564+32delinsTGGA	NP_001351656.1:n.4564+29_4564+32delinsTGGA
XM_005244749.3:c.4879+29_4879+32delinsTGGA	XP_005244806.1:n.4879+29_4879+32delinsTGGA
XM_011541429.2:c.4879+29_4879+32delinsTGGA	XP_011539731.1:n.4879+29_4879+32delinsTGGA
XR_946650.2:n.4950+29_4950+32delinsTGGA
NM_001305275.2:c.4879+29_4879+32delinsTGGA	NP_001292204.1:n.4879+29_4879+32delinsTGGA
NM_198576.4:c.4879+29_4879+32delinsTGGA MANE Select	NP_940978.2:n.4879+29_4879+32delinsTGGA
NM_001364727.2:c.4564+29_4564+32delinsTGGA	NP_001351656.1:n.4564+29_4564+32delinsTGGA