Canonical Allele Identifier: CA2574258692

Gene: AGRN

Linked Data

• ClinVar Variation Id: 2041421
• ClinVar RCV Id: RCV002891113

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1047774del , CM000663.2:g.1047774del	GRCh38
NC_000001.10:g.983154del , CM000663.1:g.983154del	GRCh37
NC_000001.9:g.973017del	NCBI36
NG_016346.1:g.32652del , LRG_198:g.32652del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.3632-2del MANE Select	ENSP00000368678.2:n.3632-2del
ENST00000651234.1:c.3317-2del	ENSP00000499046.1:n.3317-2del
ENST00000652369.1:c.3317-2del	ENSP00000498543.1:n.3317-2del
ENST00000379370.6:c.3632-2del	ENSP00000368678.2:n.3632-2del
ENST00000466223.1:n.370-2del
ENST00000478677.1:n.214-2del
ENST00000620552.4:c.3218-2del	ENSP00000484607.1:n.3218-2del
NM_001305275.1:c.3632-2del	NP_001292204.1:n.3632-2del
NM_198576.3:c.3632-2del	NP_940978.2:n.3632-2del
XM_005244749.2:c.3632-2del	XP_005244806.1:n.3632-2del
XM_006710635.2:c.3632-2del	XP_006710698.1:n.3632-2del
XM_011541429.1:c.3632-2del	XP_011539731.1:n.3632-2del
XM_011541430.1:c.2759-2del	XP_011539732.1:n.2759-2del
XM_011541431.1:c.1898-2del	XP_011539733.1:n.1898-2del
XR_946650.1:n.3699-2del
NM_001364727.1:c.3317-2del	NP_001351656.1:n.3317-2del
XM_005244749.3:c.3632-2del	XP_005244806.1:n.3632-2del
XM_011541429.2:c.3632-2del	XP_011539731.1:n.3632-2del
XR_946650.2:n.3703-2del
NM_001305275.2:c.3632-2del	NP_001292204.1:n.3632-2del
NM_198576.4:c.3632-2del MANE Select	NP_940978.2:n.3632-2del
NM_001364727.2:c.3317-2del	NP_001351656.1:n.3317-2del