Canonical Allele Identifier: CA415758928

Gene: AGRN

Linked Data

• dbSNP Id: rs115019873
• gnomAD v3: 1-1049791-C-A
• gnomAD v4: 1-1049791-C-A
• MyVariant Identifiers: chr1:g.985171C>A (hg19) ; chr1:g.1049791C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1049791C>A , CM000663.2:g.1049791C>A	GRCh38
NC_000001.10:g.985171C>A , CM000663.1:g.985171C>A	GRCh37
NC_000001.9:g.975034C>A	NCBI36
NG_016346.1:g.34669C>A , LRG_198:g.34669C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.4740C>A MANE Select	ENSP00000368678.2:p.Arg1580=
ENST00000651234.1:c.4425C>A	ENSP00000499046.1:p.Arg1475=
ENST00000652369.1:c.4425C>A	ENSP00000498543.1:p.Arg1475=
ENST00000379370.6:c.4740C>A	ENSP00000368678.2:p.Arg1580=
ENST00000620552.4:c.4326C>A	ENSP00000484607.1:p.Arg1442=
NM_001305275.1:c.4740C>A	NP_001292204.1:p.Arg1580=
NM_198576.3:c.4740C>A	NP_940978.2:p.Arg1580=
XM_005244749.2:c.4740C>A	XP_005244806.1:p.Arg1580=
XM_006710635.2:c.4740C>A	XP_006710698.1:p.Arg1580=
XM_011541429.1:c.4740C>A	XP_011539731.1:p.Arg1580=
XM_011541430.1:c.3867C>A	XP_011539732.1:p.Arg1289=
XM_011541431.1:c.3006C>A	XP_011539733.1:p.Arg1002=
XR_946650.1:n.4807C>A
NM_001364727.1:c.4425C>A	NP_001351656.1:p.Arg1475=
XM_005244749.3:c.4740C>A	XP_005244806.1:p.Arg1580=
XM_011541429.2:c.4740C>A	XP_011539731.1:p.Arg1580=
XR_946650.2:n.4811C>A
NM_001305275.2:c.4740C>A	NP_001292204.1:p.Arg1580=
NM_198576.4:c.4740C>A MANE Select	NP_940978.2:p.Arg1580=
NM_001364727.2:c.4425C>A	NP_001351656.1:p.Arg1475=