Canonical Allele Identifier: CA1148747606

Gene: AGRN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1049957_1049958delinsCG , CM000663.2:g.1049957_1049958delinsCG	GRCh38
NC_000001.10:g.985337_985338delinsCG , CM000663.1:g.985337_985338delinsCG	GRCh37
NC_000001.9:g.975200_975201delinsCG	NCBI36
NG_016346.1:g.34835_34836delinsCG , LRG_198:g.34835_34836delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.4799_4800delinsCG MANE Select	ENSP00000368678.2:p.Ala1600=
ENST00000651234.1:c.4484_4485delinsCG	ENSP00000499046.1:p.Ala1495=
ENST00000652369.1:c.4484_4485delinsCG	ENSP00000498543.1:p.Ala1495=
ENST00000379370.6:c.4799_4800delinsCG	ENSP00000368678.2:p.Ala1600=
ENST00000620552.4:c.4385_4386delinsCG	ENSP00000484607.1:p.Ala1462=
NM_001305275.1:c.4799_4800delinsCG	NP_001292204.1:p.Ala1600=
NM_198576.3:c.4799_4800delinsCG	NP_940978.2:p.Ala1600=
XM_005244749.2:c.4799_4800delinsCG	XP_005244806.1:p.Ala1600=
XM_006710635.2:c.4799_4800delinsCG	XP_006710698.1:p.Ala1600=
XM_011541429.1:c.4799_4800delinsCG	XP_011539731.1:p.Ala1600=
XM_011541430.1:c.3926_3927delinsCG	XP_011539732.1:p.Ala1309=
XM_011541431.1:c.3065_3066delinsCG	XP_011539733.1:p.Ala1022=
XR_946650.1:n.4866_4867delinsCG
NM_001364727.1:c.4484_4485delinsCG	NP_001351656.1:p.Ala1495=
XM_005244749.3:c.4799_4800delinsCG	XP_005244806.1:p.Ala1600=
XM_011541429.2:c.4799_4800delinsCG	XP_011539731.1:p.Ala1600=
XR_946650.2:n.4870_4871delinsCG
NM_001305275.2:c.4799_4800delinsCG	NP_001292204.1:p.Ala1600=
NM_198576.4:c.4799_4800delinsCG MANE Select	NP_940978.2:p.Ala1600=
NM_001364727.2:c.4484_4485delinsCG	NP_001351656.1:p.Ala1495=