Canonical Allele Identifier: CA509358

Gene: AGRN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1048978_1048979del , CM000663.2:g.1048978_1048979del	GRCh38
NC_000001.10:g.984358_984359del , CM000663.1:g.984358_984359del	GRCh37
NC_000001.9:g.974221_974222del	NCBI36
NG_016346.1:g.33856_33857del , LRG_198:g.33856_33857del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.4217_4218del MANE Select	ENSP00000368678.2:p.Gln1406ArgfsTer29
ENST00000651234.1:c.3902_3903del	ENSP00000499046.1:p.Gln1301ArgfsTer29
ENST00000652369.1:c.3902_3903del	ENSP00000498543.1:p.Gln1301ArgfsTer29
ENST00000379370.6:c.4217_4218del	ENSP00000368678.2:p.Gln1406ArgfsTer29
ENST00000492947.1:n.450_451del
ENST00000620552.4:c.3803_3804del	ENSP00000484607.1:p.Gln1268ArgfsTer29
NM_001305275.1:c.4217_4218del	NP_001292204.1:p.Gln1406ArgfsTer29
NM_198576.3:c.4217_4218del	NP_940978.2:p.Gln1406ArgfsTer29
XM_005244749.2:c.4217_4218del	XP_005244806.1:p.Gln1406ArgfsTer29
XM_006710635.2:c.4217_4218del	XP_006710698.1:p.Gln1406ArgfsTer29
XM_011541429.1:c.4217_4218del	XP_011539731.1:p.Gln1406ArgfsTer29
XM_011541430.1:c.3344_3345del	XP_011539732.1:p.Gln1115ArgfsTer29
XM_011541431.1:c.2483_2484del	XP_011539733.1:p.Gln828ArgfsTer29
XR_946650.1:n.4284_4285del
NM_001364727.1:c.3902_3903del	NP_001351656.1:p.Gln1301ArgfsTer29
XM_005244749.3:c.4217_4218del	XP_005244806.1:p.Gln1406ArgfsTer29
XM_011541429.2:c.4217_4218del	XP_011539731.1:p.Gln1406ArgfsTer29
XR_946650.2:n.4288_4289del
NM_001305275.2:c.4217_4218del	NP_001292204.1:p.Gln1406ArgfsTer29
NM_198576.4:c.4217_4218del MANE Select	NP_940978.2:p.Gln1406ArgfsTer29
NM_001364727.2:c.3902_3903del	NP_001351656.1:p.Gln1301ArgfsTer29