Canonical Allele Identifier: CA337779811

Gene: AGRN

Linked Data

• MyVariant Identifiers: chr1:g.1050348del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1050352del , CM000663.2:g.1050352del	GRCh38
NC_000001.10:g.985732del , CM000663.1:g.985732del	GRCh37
NC_000001.9:g.975595del	NCBI36
NG_016346.1:g.35230del , LRG_198:g.35230del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.4976+23del MANE Select	ENSP00000368678.2:n.4976+23del
ENST00000651234.1:c.4661+23del	ENSP00000499046.1:n.4661+23del
ENST00000652369.1:c.4661+23del	ENSP00000498543.1:n.4661+23del
ENST00000379370.6:c.4976+23del	ENSP00000368678.2:n.4976+23del
ENST00000620552.4:c.4562+23del	ENSP00000484607.1:n.4562+23del
NM_001305275.1:c.4976+23del	NP_001292204.1:n.4976+23del
NM_198576.3:c.4976+23del	NP_940978.2:n.4976+23del
XM_005244749.2:c.4976+23del	XP_005244806.1:n.4976+23del
XM_006710635.2:c.4976+23del	XP_006710698.1:n.4976+23del
XM_011541429.1:c.4976+23del	XP_011539731.1:n.4976+23del
XM_011541430.1:c.4103+23del	XP_011539732.1:n.4103+23del
XM_011541431.1:c.3242+23del	XP_011539733.1:n.3242+23del
XR_946650.1:n.5043+23del
NM_001364727.1:c.4661+23del	NP_001351656.1:n.4661+23del
XM_005244749.3:c.4976+23del	XP_005244806.1:n.4976+23del
XM_011541429.2:c.4976+23del	XP_011539731.1:n.4976+23del
XR_946650.2:n.5047+23del
NM_001305275.2:c.4976+23del	NP_001292204.1:n.4976+23del
NM_198576.4:c.4976+23del MANE Select	NP_940978.2:n.4976+23del
NM_001364727.2:c.4661+23del	NP_001351656.1:n.4661+23del