Canonical Allele Identifier: CA337779694

Gene: AGRN

Linked Data

• dbSNP Id: rs1570244154
• gnomAD v4: 1-1050275-A-G
• MyVariant Identifiers: chr1:g.985655A>G (hg19) ; chr1:g.1050275A>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.4922A>G MANE Select	ENSP00000368678.2:p.Asn1641Ser
ENST00000651234.1:c.4607A>G	ENSP00000499046.1:p.Asn1536Ser
ENST00000652369.1:c.4607A>G	ENSP00000498543.1:p.Asn1536Ser
ENST00000379370.6:c.4922A>G	ENSP00000368678.2:p.Asn1641Ser
ENST00000620552.4:c.4508A>G	ENSP00000484607.1:p.Asn1503Ser
NM_001305275.1:c.4922A>G	NP_001292204.1:p.Asn1641Ser
NM_198576.3:c.4922A>G	NP_940978.2:p.Asn1641Ser
XM_005244749.2:c.4922A>G	XP_005244806.1:p.Asn1641Ser
XM_006710635.2:c.4922A>G	XP_006710698.1:p.Asn1641Ser
XM_011541429.1:c.4922A>G	XP_011539731.1:p.Asn1641Ser
XM_011541430.1:c.4049A>G	XP_011539732.1:p.Asn1350Ser
XM_011541431.1:c.3188A>G	XP_011539733.1:p.Asn1063Ser
XR_946650.1:n.4989A>G
NM_001364727.1:c.4607A>G	NP_001351656.1:p.Asn1536Ser
XM_005244749.3:c.4922A>G	XP_005244806.1:p.Asn1641Ser
XM_011541429.2:c.4922A>G	XP_011539731.1:p.Asn1641Ser
XR_946650.2:n.4993A>G
NM_001305275.2:c.4922A>G	NP_001292204.1:p.Asn1641Ser
NM_198576.4:c.4922A>G MANE Select	NP_940978.2:p.Asn1641Ser
NM_001364727.2:c.4607A>G	NP_001351656.1:p.Asn1536Ser