Canonical Allele Identifier: CA509303

Gene: AGRN

Linked Data

• ClinVar Variation Id: 1363310
• ClinVar RCV Id: RCV001902189
• dbSNP Id: rs750911464
• ExAC: 1:983690 C / T
• gnomAD v2: 1-983690-C-T
• gnomAD v3: 1-1048310-C-T
• gnomAD v4: 1-1048310-C-T
• MyVariant Identifiers: chr1:g.983690C>T (hg19) ; chr1:g.983690_983691delinsTG (hg19) ; chr1:g.1048310C>T (hg38) ; chr1:g.1048310_1048311delinsTG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1048310C>T , CM000663.2:g.1048310C>T	GRCh38
NC_000001.10:g.983690C>T , CM000663.1:g.983690C>T	GRCh37
NC_000001.9:g.973553C>T	NCBI36
NG_016346.1:g.33188C>T , LRG_198:g.33188C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.4050C>T MANE Select	ENSP00000368678.2:p.Gly1350=
ENST00000651234.1:c.3735C>T	ENSP00000499046.1:p.Gly1245=
ENST00000652369.1:c.3735C>T	ENSP00000498543.1:p.Gly1245=
ENST00000379370.6:c.4050C>T	ENSP00000368678.2:p.Gly1350=
ENST00000620552.4:c.3636C>T	ENSP00000484607.1:p.Gly1212=
NM_001305275.1:c.4050C>T	NP_001292204.1:p.Gly1350=
NM_198576.3:c.4050C>T	NP_940978.2:p.Gly1350=
XM_005244749.2:c.4050C>T	XP_005244806.1:p.Gly1350=
XM_006710635.2:c.4050C>T	XP_006710698.1:p.Gly1350=
XM_011541429.1:c.4050C>T	XP_011539731.1:p.Gly1350=
XM_011541430.1:c.3177C>T	XP_011539732.1:p.Gly1059=
XM_011541431.1:c.2316C>T	XP_011539733.1:p.Gly772=
XR_946650.1:n.4117C>T
NM_001364727.1:c.3735C>T	NP_001351656.1:p.Gly1245=
XM_005244749.3:c.4050C>T	XP_005244806.1:p.Gly1350=
XM_011541429.2:c.4050C>T	XP_011539731.1:p.Gly1350=
XR_946650.2:n.4121C>T
NM_001305275.2:c.4050C>T	NP_001292204.1:p.Gly1350=
NM_198576.4:c.4050C>T MANE Select	NP_940978.2:p.Gly1350=
NM_001364727.2:c.3735C>T	NP_001351656.1:p.Gly1245=