Canonical Allele Identifier: CA2499214097

Gene: AGRN

Linked Data

• ClinVar Variation Id: 1177400
• ClinVar RCV Id: RCV002051720
• dbSNP Id: rs2100682020

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1050275dup , CM000663.2:g.1050275dup	GRCh38
NC_000001.10:g.985655dup , CM000663.1:g.985655dup	GRCh37
NC_000001.9:g.975518dup	NCBI36
NG_016346.1:g.35153dup , LRG_198:g.35153dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.4922dup MANE Select	ENSP00000368678.2:p.Asn1641LysfsTer?
ENST00000651234.1:c.4607dup	ENSP00000499046.1:p.Asn1536LysfsTer?
ENST00000652369.1:c.4607dup	ENSP00000498543.1:p.Asn1536LysfsTer?
ENST00000379370.6:c.4922dup	ENSP00000368678.2:p.Asn1641LysfsTer?
ENST00000620552.4:c.4508dup	ENSP00000484607.1:p.Asn1503LysfsTer?
NM_001305275.1:c.4922dup	NP_001292204.1:p.Asn1641LysfsTer?
NM_198576.3:c.4922dup	NP_940978.2:p.Asn1641LysfsTer?
XM_005244749.2:c.4922dup	XP_005244806.1:p.Asn1641LysfsTer?
XM_006710635.2:c.4922dup	XP_006710698.1:p.Asn1641LysfsTer?
XM_011541429.1:c.4922dup	XP_011539731.1:p.Asn1641LysfsTer?
XM_011541430.1:c.4049dup	XP_011539732.1:p.Asn1350LysfsTer?
XM_011541431.1:c.3188dup	XP_011539733.1:p.Asn1063LysfsTer?
XR_946650.1:n.4989dup
NM_001364727.1:c.4607dup	NP_001351656.1:p.Asn1536LysfsTer?
XM_005244749.3:c.4922dup	XP_005244806.1:p.Asn1641LysfsTer?
XM_011541429.2:c.4922dup	XP_011539731.1:p.Asn1641LysfsTer?
XR_946650.2:n.4993dup
NM_001305275.2:c.4922dup	NP_001292204.1:p.Asn1641LysfsTer?
NM_198576.4:c.4922dup MANE Select	NP_940978.2:p.Asn1641LysfsTer?
NM_001364727.2:c.4607dup	NP_001351656.1:p.Asn1536LysfsTer?