Canonical Allele Identifier: CA1148802628

Gene: AGRN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1047891_1047892delinsCT , CM000663.2:g.1047891_1047892delinsCT	GRCh38
NC_000001.10:g.983271_983272delinsCT , CM000663.1:g.983271_983272delinsCT	GRCh37
NC_000001.9:g.973134_973135delinsCT	NCBI36
NG_016346.1:g.32769_32770delinsCT , LRG_198:g.32769_32770delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.3747_3748delinsCT MANE Select	ENSP00000368678.2:p.Asp1249=
ENST00000651234.1:c.3432_3433delinsCT	ENSP00000499046.1:p.Asp1144=
ENST00000652369.1:c.3432_3433delinsCT	ENSP00000498543.1:p.Asp1144=
ENST00000379370.6:c.3747_3748delinsCT	ENSP00000368678.2:p.Asp1249=
ENST00000620552.4:c.3333_3334delinsCT	ENSP00000484607.1:p.Asp1111=
NM_001305275.1:c.3747_3748delinsCT	NP_001292204.1:p.Asp1249=
NM_198576.3:c.3747_3748delinsCT	NP_940978.2:p.Asp1249=
XM_005244749.2:c.3747_3748delinsCT	XP_005244806.1:p.Asp1249=
XM_006710635.2:c.3747_3748delinsCT	XP_006710698.1:p.Asp1249=
XM_011541429.1:c.3747_3748delinsCT	XP_011539731.1:p.Asp1249=
XM_011541430.1:c.2874_2875delinsCT	XP_011539732.1:p.Asp958=
XM_011541431.1:c.2013_2014delinsCT	XP_011539733.1:p.Asp671=
XR_946650.1:n.3814_3815delinsCT
NM_001364727.1:c.3432_3433delinsCT	NP_001351656.1:p.Asp1144=
XM_005244749.3:c.3747_3748delinsCT	XP_005244806.1:p.Asp1249=
XM_011541429.2:c.3747_3748delinsCT	XP_011539731.1:p.Asp1249=
XR_946650.2:n.3818_3819delinsCT
NM_001305275.2:c.3747_3748delinsCT	NP_001292204.1:p.Asp1249=
NM_198576.4:c.3747_3748delinsCT MANE Select	NP_940978.2:p.Asp1249=
NM_001364727.2:c.3432_3433delinsCT	NP_001351656.1:p.Asp1144=