Canonical Allele Identifier: CA2642490973

Gene: AGRN

Linked Data

• gnomAD v4: 1-1044098-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1044100del , CM000663.2:g.1044100del	GRCh38
NC_000001.10:g.979480del , CM000663.1:g.979480del	GRCh37
NC_000001.9:g.969343del	NCBI36
NG_016346.1:g.28978del , LRG_198:g.28978del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.2000-9del MANE Select	ENSP00000368678.2:n.2000-9del
ENST00000651234.1:c.1685-9del	ENSP00000499046.1:n.1685-9del
ENST00000652369.1:c.1685-9del	ENSP00000498543.1:n.1685-9del
ENST00000379370.6:c.2000-9del	ENSP00000368678.2:n.2000-9del
ENST00000620552.4:c.1586-9del	ENSP00000484607.1:n.1586-9del
NM_001305275.1:c.2000-9del	NP_001292204.1:n.2000-9del
NM_198576.3:c.2000-9del	NP_940978.2:n.2000-9del
XM_005244749.2:c.2000-9del	XP_005244806.1:n.2000-9del
XM_006710635.2:c.2000-9del	XP_006710698.1:n.2000-9del
XM_011541429.1:c.2000-9del	XP_011539731.1:n.2000-9del
XM_011541430.1:c.1127-9del	XP_011539732.1:n.1127-9del
XM_011541431.1:c.266-9del	XP_011539733.1:n.266-9del
XR_946650.1:n.2067-9del
NM_001364727.1:c.1685-9del	NP_001351656.1:n.1685-9del
XM_005244749.3:c.2000-9del	XP_005244806.1:n.2000-9del
XM_011541429.2:c.2000-9del	XP_011539731.1:n.2000-9del
XR_946650.2:n.2071-9del
NM_001305275.2:c.2000-9del	NP_001292204.1:n.2000-9del
NM_198576.4:c.2000-9del MANE Select	NP_940978.2:n.2000-9del
NM_001364727.2:c.1685-9del	NP_001351656.1:n.1685-9del