Canonical Allele Identifier: CA1148804346

Gene: AGRN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1048187_1048188delinsGC , CM000663.2:g.1048187_1048188delinsGC	GRCh38
NC_000001.10:g.983567_983568delinsGC , CM000663.1:g.983567_983568delinsGC	GRCh37
NC_000001.9:g.973430_973431delinsGC	NCBI36
NG_016346.1:g.33065_33066delinsGC , LRG_198:g.33065_33066delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.3927_3928delinsGC MANE Select	ENSP00000368678.2:p.Arg1309=
ENST00000651234.1:c.3612_3613delinsGC	ENSP00000499046.1:p.Arg1204=
ENST00000652369.1:c.3612_3613delinsGC	ENSP00000498543.1:p.Arg1204=
ENST00000379370.6:c.3927_3928delinsGC	ENSP00000368678.2:p.Arg1309=
ENST00000620552.4:c.3513_3514delinsGC	ENSP00000484607.1:p.Arg1171=
NM_001305275.1:c.3927_3928delinsGC	NP_001292204.1:p.Arg1309=
NM_198576.3:c.3927_3928delinsGC	NP_940978.2:p.Arg1309=
XM_005244749.2:c.3927_3928delinsGC	XP_005244806.1:p.Arg1309=
XM_006710635.2:c.3927_3928delinsGC	XP_006710698.1:p.Arg1309=
XM_011541429.1:c.3927_3928delinsGC	XP_011539731.1:p.Arg1309=
XM_011541430.1:c.3054_3055delinsGC	XP_011539732.1:p.Arg1018=
XM_011541431.1:c.2193_2194delinsGC	XP_011539733.1:p.Arg731=
XR_946650.1:n.3994_3995delinsGC
NM_001364727.1:c.3612_3613delinsGC	NP_001351656.1:p.Arg1204=
XM_005244749.3:c.3927_3928delinsGC	XP_005244806.1:p.Arg1309=
XM_011541429.2:c.3927_3928delinsGC	XP_011539731.1:p.Arg1309=
XR_946650.2:n.3998_3999delinsGC
NM_001305275.2:c.3927_3928delinsGC	NP_001292204.1:p.Arg1309=
NM_198576.4:c.3927_3928delinsGC MANE Select	NP_940978.2:p.Arg1309=
NM_001364727.2:c.3612_3613delinsGC	NP_001351656.1:p.Arg1204=