Canonical Allele Identifier: CA2642497052

Gene: AGRN

Linked Data

• gnomAD v4: 1-1049802-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1049803del , CM000663.2:g.1049803del	GRCh38
NC_000001.10:g.985183del , CM000663.1:g.985183del	GRCh37
NC_000001.9:g.975046del	NCBI36
NG_016346.1:g.34681del , LRG_198:g.34681del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.4744+8del MANE Select	ENSP00000368678.2:n.4744+8del
ENST00000651234.1:c.4429+8del	ENSP00000499046.1:n.4429+8del
ENST00000652369.1:c.4429+8del	ENSP00000498543.1:n.4429+8del
ENST00000379370.6:c.4744+8del	ENSP00000368678.2:n.4744+8del
ENST00000620552.4:c.4330+8del	ENSP00000484607.1:n.4330+8del
NM_001305275.1:c.4744+8del	NP_001292204.1:n.4744+8del
NM_198576.3:c.4744+8del	NP_940978.2:n.4744+8del
XM_005244749.2:c.4744+8del	XP_005244806.1:n.4744+8del
XM_006710635.2:c.4744+8del	XP_006710698.1:n.4744+8del
XM_011541429.1:c.4744+8del	XP_011539731.1:n.4744+8del
XM_011541430.1:c.3871+8del	XP_011539732.1:n.3871+8del
XM_011541431.1:c.3010+8del	XP_011539733.1:n.3010+8del
XR_946650.1:n.4811+8del
NM_001364727.1:c.4429+8del	NP_001351656.1:n.4429+8del
XM_005244749.3:c.4744+8del	XP_005244806.1:n.4744+8del
XM_011541429.2:c.4744+8del	XP_011539731.1:n.4744+8del
XR_946650.2:n.4815+8del
NM_001305275.2:c.4744+8del	NP_001292204.1:n.4744+8del
NM_198576.4:c.4744+8del MANE Select	NP_940978.2:n.4744+8del
NM_001364727.2:c.4429+8del	NP_001351656.1:n.4429+8del