Canonical Allele Identifier: CA509283

Gene: AGRN

Linked Data

• dbSNP Id: rs763455187
• ExAC: 1:983581 C / T
• gnomAD v2: 1-983581-C-T
• gnomAD v4: 1-1048201-C-T
• MyVariant Identifiers: chr1:g.983581C>T (hg19) ; chr1:g.1048201C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1048201C>T , CM000663.2:g.1048201C>T	GRCh38
NC_000001.10:g.983581C>T , CM000663.1:g.983581C>T	GRCh37
NC_000001.9:g.973444C>T	NCBI36
NG_016346.1:g.33079C>T , LRG_198:g.33079C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.3941C>T MANE Select	ENSP00000368678.2:p.Ala1314Val
ENST00000651234.1:c.3626C>T	ENSP00000499046.1:p.Ala1209Val
ENST00000652369.1:c.3626C>T	ENSP00000498543.1:p.Ala1209Val
ENST00000379370.6:c.3941C>T	ENSP00000368678.2:p.Ala1314Val
ENST00000620552.4:c.3527C>T	ENSP00000484607.1:p.Ala1176Val
NM_001305275.1:c.3941C>T	NP_001292204.1:p.Ala1314Val
NM_198576.3:c.3941C>T	NP_940978.2:p.Ala1314Val
XM_005244749.2:c.3941C>T	XP_005244806.1:p.Ala1314Val
XM_006710635.2:c.3941C>T	XP_006710698.1:p.Ala1314Val
XM_011541429.1:c.3941C>T	XP_011539731.1:p.Ala1314Val
XM_011541430.1:c.3068C>T	XP_011539732.1:p.Ala1023Val
XM_011541431.1:c.2207C>T	XP_011539733.1:p.Ala736Val
XR_946650.1:n.4008C>T
NM_001364727.1:c.3626C>T	NP_001351656.1:p.Ala1209Val
XM_005244749.3:c.3941C>T	XP_005244806.1:p.Ala1314Val
XM_011541429.2:c.3941C>T	XP_011539731.1:p.Ala1314Val
XR_946650.2:n.4012C>T
NM_001305275.2:c.3941C>T	NP_001292204.1:p.Ala1314Val
NM_198576.4:c.3941C>T MANE Select	NP_940978.2:p.Ala1314Val
NM_001364727.2:c.3626C>T	NP_001351656.1:p.Ala1209Val