Canonical Allele Identifier: CA2642491942

Gene: AGRN

Linked Data

• gnomAD v4: 1-1047848-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1047853del , CM000663.2:g.1047853del	GRCh38
NC_000001.10:g.983233del , CM000663.1:g.983233del	GRCh37
NC_000001.9:g.973096del	NCBI36
NG_016346.1:g.32731del , LRG_198:g.32731del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.3709del MANE Select	ENSP00000368678.2:p.Val1237Ter
ENST00000651234.1:c.3394del	ENSP00000499046.1:p.Val1132Ter
ENST00000652369.1:c.3394del	ENSP00000498543.1:p.Val1132Ter
ENST00000379370.6:c.3709del	ENSP00000368678.2:p.Val1237Ter
ENST00000466223.1:n.447del
ENST00000620552.4:c.3295del	ENSP00000484607.1:p.Val1099Ter
NM_001305275.1:c.3709del	NP_001292204.1:p.Val1237Ter
NM_198576.3:c.3709del	NP_940978.2:p.Val1237Ter
XM_005244749.2:c.3709del	XP_005244806.1:p.Val1237Ter
XM_006710635.2:c.3709del	XP_006710698.1:p.Val1237Ter
XM_011541429.1:c.3709del	XP_011539731.1:p.Val1237Ter
XM_011541430.1:c.2836del	XP_011539732.1:p.Val946Ter
XM_011541431.1:c.1975del	XP_011539733.1:p.Val659Ter
XR_946650.1:n.3776del
NM_001364727.1:c.3394del	NP_001351656.1:p.Val1132Ter
XM_005244749.3:c.3709del	XP_005244806.1:p.Val1237Ter
XM_011541429.2:c.3709del	XP_011539731.1:p.Val1237Ter
XR_946650.2:n.3780del
NM_001305275.2:c.3709del	NP_001292204.1:p.Val1237Ter
NM_198576.4:c.3709del MANE Select	NP_940978.2:p.Val1237Ter
NM_001364727.2:c.3394del	NP_001351656.1:p.Val1132Ter