Canonical Allele Identifier: CA16759844

Gene: AGRN

Linked Data

• dbSNP Id: rs35467258

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1047819del , CM000663.2:g.1047819del	GRCh38
NC_000001.10:g.983199del , CM000663.1:g.983199del	GRCh37
NC_000001.9:g.973062del	NCBI36
NG_016346.1:g.32697del , LRG_198:g.32697del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.3675del MANE Select	ENSP00000368678.2:p.Gln1226ArgfsTer12
ENST00000651234.1:c.3360del	ENSP00000499046.1:p.Gln1121ArgfsTer12
ENST00000652369.1:c.3360del	ENSP00000498543.1:p.Gln1121ArgfsTer12
ENST00000379370.6:c.3675del	ENSP00000368678.2:p.Gln1226ArgfsTer12
ENST00000466223.1:n.413del
ENST00000478677.1:n.257del
ENST00000620552.4:c.3261del	ENSP00000484607.1:p.Gln1088ArgfsTer12
NM_001305275.1:c.3675del	NP_001292204.1:p.Gln1226ArgfsTer12
NM_198576.3:c.3675del	NP_940978.2:p.Gln1226ArgfsTer12
XM_005244749.2:c.3675del	XP_005244806.1:p.Gln1226ArgfsTer12
XM_006710635.2:c.3675del	XP_006710698.1:p.Gln1226ArgfsTer12
XM_011541429.1:c.3675del	XP_011539731.1:p.Gln1226ArgfsTer12
XM_011541430.1:c.2802del	XP_011539732.1:p.Gln935ArgfsTer12
XM_011541431.1:c.1941del	XP_011539733.1:p.Gln648ArgfsTer12
XR_946650.1:n.3742del
NM_001364727.1:c.3360del	NP_001351656.1:p.Gln1121ArgfsTer12
XM_005244749.3:c.3675del	XP_005244806.1:p.Gln1226ArgfsTer12
XM_011541429.2:c.3675del	XP_011539731.1:p.Gln1226ArgfsTer12
XR_946650.2:n.3746del
NM_001305275.2:c.3675del	NP_001292204.1:p.Gln1226ArgfsTer12
NM_198576.4:c.3675del MANE Select	NP_940978.2:p.Gln1226ArgfsTer12
NM_001364727.2:c.3360del	NP_001351656.1:p.Gln1121ArgfsTer12