Canonical Allele Identifier: CA520659051

Gene: AGRN

Linked Data

• dbSNP Id: rs1356351416
• gnomAD v2: 1-983108-TG-T
• gnomAD v4: 1-1047728-TG-T
• MyVariant Identifiers: chr1:g.983109del (hg19) ; chr1:g.1047729del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1047733del , CM000663.2:g.1047733del	GRCh38
NC_000001.10:g.983113del , CM000663.1:g.983113del	GRCh37
NC_000001.9:g.972976del	NCBI36
NG_016346.1:g.32611del , LRG_198:g.32611del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.3632-43del MANE Select	ENSP00000368678.2:n.3632-43del
ENST00000651234.1:c.3317-43del	ENSP00000499046.1:n.3317-43del
ENST00000652369.1:c.3317-43del	ENSP00000498543.1:n.3317-43del
ENST00000379370.6:c.3632-43del	ENSP00000368678.2:n.3632-43del
ENST00000466223.1:n.370-43del
ENST00000478677.1:n.214-43del
ENST00000620552.4:c.3218-43del	ENSP00000484607.1:n.3218-43del
NM_001305275.1:c.3632-43del	NP_001292204.1:n.3632-43del
NM_198576.3:c.3632-43del	NP_940978.2:n.3632-43del
XM_005244749.2:c.3632-43del	XP_005244806.1:n.3632-43del
XM_006710635.2:c.3632-43del	XP_006710698.1:n.3632-43del
XM_011541429.1:c.3632-43del	XP_011539731.1:n.3632-43del
XM_011541430.1:c.2759-43del	XP_011539732.1:n.2759-43del
XM_011541431.1:c.1898-43del	XP_011539733.1:n.1898-43del
XR_946650.1:n.3699-43del
NM_001364727.1:c.3317-43del	NP_001351656.1:n.3317-43del
XM_005244749.3:c.3632-43del	XP_005244806.1:n.3632-43del
XM_011541429.2:c.3632-43del	XP_011539731.1:n.3632-43del
XR_946650.2:n.3703-43del
NM_001305275.2:c.3632-43del	NP_001292204.1:n.3632-43del
NM_198576.4:c.3632-43del MANE Select	NP_940978.2:n.3632-43del
NM_001364727.2:c.3317-43del	NP_001351656.1:n.3317-43del