Canonical Allele Identifier: CA1148804948

Gene: AGRN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1048233_1048234delinsGC , CM000663.2:g.1048233_1048234delinsGC	GRCh38
NC_000001.10:g.983613_983614delinsGC , CM000663.1:g.983613_983614delinsGC	GRCh37
NC_000001.9:g.973476_973477delinsGC	NCBI36
NG_016346.1:g.33111_33112delinsGC , LRG_198:g.33111_33112delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.3973_3974delinsGC MANE Select	ENSP00000368678.2:p.Ala1325=
ENST00000651234.1:c.3658_3659delinsGC	ENSP00000499046.1:p.Ala1220=
ENST00000652369.1:c.3658_3659delinsGC	ENSP00000498543.1:p.Ala1220=
ENST00000379370.6:c.3973_3974delinsGC	ENSP00000368678.2:p.Ala1325=
ENST00000620552.4:c.3559_3560delinsGC	ENSP00000484607.1:p.Ala1187=
NM_001305275.1:c.3973_3974delinsGC	NP_001292204.1:p.Ala1325=
NM_198576.3:c.3973_3974delinsGC	NP_940978.2:p.Ala1325=
XM_005244749.2:c.3973_3974delinsGC	XP_005244806.1:p.Ala1325=
XM_006710635.2:c.3973_3974delinsGC	XP_006710698.1:p.Ala1325=
XM_011541429.1:c.3973_3974delinsGC	XP_011539731.1:p.Ala1325=
XM_011541430.1:c.3100_3101delinsGC	XP_011539732.1:p.Ala1034=
XM_011541431.1:c.2239_2240delinsGC	XP_011539733.1:p.Ala747=
XR_946650.1:n.4040_4041delinsGC
NM_001364727.1:c.3658_3659delinsGC	NP_001351656.1:p.Ala1220=
XM_005244749.3:c.3973_3974delinsGC	XP_005244806.1:p.Ala1325=
XM_011541429.2:c.3973_3974delinsGC	XP_011539731.1:p.Ala1325=
XR_946650.2:n.4044_4045delinsGC
NM_001305275.2:c.3973_3974delinsGC	NP_001292204.1:p.Ala1325=
NM_198576.4:c.3973_3974delinsGC MANE Select	NP_940978.2:p.Ala1325=
NM_001364727.2:c.3658_3659delinsGC	NP_001351656.1:p.Ala1220=