Canonical Allele Identifier: CA1148746476

Gene: AGRN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1049828_1049829delinsAC , CM000663.2:g.1049828_1049829delinsAC	GRCh38
NC_000001.10:g.985208_985209delinsAC , CM000663.1:g.985208_985209delinsAC	GRCh37
NC_000001.9:g.975071_975072delinsAC	NCBI36
NG_016346.1:g.34706_34707delinsAC , LRG_198:g.34706_34707delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.4744+33_4744+34delinsAC MANE Select	ENSP00000368678.2:n.4744+33_4744+34delinsAC
ENST00000651234.1:c.4429+33_4429+34delinsAC	ENSP00000499046.1:n.4429+33_4429+34delinsAC
ENST00000652369.1:c.4429+33_4429+34delinsAC	ENSP00000498543.1:n.4429+33_4429+34delinsAC
ENST00000379370.6:c.4744+33_4744+34delinsAC	ENSP00000368678.2:n.4744+33_4744+34delinsAC
ENST00000620552.4:c.4330+33_4330+34delinsAC	ENSP00000484607.1:n.4330+33_4330+34delinsAC
NM_001305275.1:c.4744+33_4744+34delinsAC	NP_001292204.1:n.4744+33_4744+34delinsAC
NM_198576.3:c.4744+33_4744+34delinsAC	NP_940978.2:n.4744+33_4744+34delinsAC
XM_005244749.2:c.4744+33_4744+34delinsAC	XP_005244806.1:n.4744+33_4744+34delinsAC
XM_006710635.2:c.4744+33_4744+34delinsAC	XP_006710698.1:n.4744+33_4744+34delinsAC
XM_011541429.1:c.4744+33_4744+34delinsAC	XP_011539731.1:n.4744+33_4744+34delinsAC
XM_011541430.1:c.3871+33_3871+34delinsAC	XP_011539732.1:n.3871+33_3871+34delinsAC
XM_011541431.1:c.3010+33_3010+34delinsAC	XP_011539733.1:n.3010+33_3010+34delinsAC
XR_946650.1:n.4811+33_4811+34delinsAC
NM_001364727.1:c.4429+33_4429+34delinsAC	NP_001351656.1:n.4429+33_4429+34delinsAC
XM_005244749.3:c.4744+33_4744+34delinsAC	XP_005244806.1:n.4744+33_4744+34delinsAC
XM_011541429.2:c.4744+33_4744+34delinsAC	XP_011539731.1:n.4744+33_4744+34delinsAC
XR_946650.2:n.4815+33_4815+34delinsAC
NM_001305275.2:c.4744+33_4744+34delinsAC	NP_001292204.1:n.4744+33_4744+34delinsAC
NM_198576.4:c.4744+33_4744+34delinsAC MANE Select	NP_940978.2:n.4744+33_4744+34delinsAC
NM_001364727.2:c.4429+33_4429+34delinsAC	NP_001351656.1:n.4429+33_4429+34delinsAC