Canonical Allele Identifier: CA1148802913

Gene: AGRN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1047933_1047934delinsCT , CM000663.2:g.1047933_1047934delinsCT	GRCh38
NC_000001.10:g.983313_983314delinsCT , CM000663.1:g.983313_983314delinsCT	GRCh37
NC_000001.9:g.973176_973177delinsCT	NCBI36
NG_016346.1:g.32811_32812delinsCT , LRG_198:g.32811_32812delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.3751+38_3751+39delinsCT MANE Select	ENSP00000368678.2:n.3751+38_3751+39delinsCT
ENST00000651234.1:c.3436+38_3436+39delinsCT	ENSP00000499046.1:n.3436+38_3436+39delinsCT
ENST00000652369.1:c.3436+38_3436+39delinsCT	ENSP00000498543.1:n.3436+38_3436+39delinsCT
ENST00000379370.6:c.3751+38_3751+39delinsCT	ENSP00000368678.2:n.3751+38_3751+39delinsCT
ENST00000620552.4:c.3337+38_3337+39delinsCT	ENSP00000484607.1:n.3337+38_3337+39delinsCT
NM_001305275.1:c.3751+38_3751+39delinsCT	NP_001292204.1:n.3751+38_3751+39delinsCT
NM_198576.3:c.3751+38_3751+39delinsCT	NP_940978.2:n.3751+38_3751+39delinsCT
XM_005244749.2:c.3751+38_3751+39delinsCT	XP_005244806.1:n.3751+38_3751+39delinsCT
XM_006710635.2:c.3751+38_3751+39delinsCT	XP_006710698.1:n.3751+38_3751+39delinsCT
XM_011541429.1:c.3751+38_3751+39delinsCT	XP_011539731.1:n.3751+38_3751+39delinsCT
XM_011541430.1:c.2878+38_2878+39delinsCT	XP_011539732.1:n.2878+38_2878+39delinsCT
XM_011541431.1:c.2017+38_2017+39delinsCT	XP_011539733.1:n.2017+38_2017+39delinsCT
XR_946650.1:n.3818+38_3818+39delinsCT
NM_001364727.1:c.3436+38_3436+39delinsCT	NP_001351656.1:n.3436+38_3436+39delinsCT
XM_005244749.3:c.3751+38_3751+39delinsCT	XP_005244806.1:n.3751+38_3751+39delinsCT
XM_011541429.2:c.3751+38_3751+39delinsCT	XP_011539731.1:n.3751+38_3751+39delinsCT
XR_946650.2:n.3822+38_3822+39delinsCT
NM_001305275.2:c.3751+38_3751+39delinsCT	NP_001292204.1:n.3751+38_3751+39delinsCT
NM_198576.4:c.3751+38_3751+39delinsCT MANE Select	NP_940978.2:n.3751+38_3751+39delinsCT
NM_001364727.2:c.3436+38_3436+39delinsCT	NP_001351656.1:n.3436+38_3436+39delinsCT