Canonical Allele Identifier: CA337853420

Gene: AGRN

Linked Data

• gnomAD v4: 1-1048318-T-A
• MyVariant Identifiers: chr1:g.983698T>A (hg19) ; chr1:g.1048318T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1048318T>A , CM000663.2:g.1048318T>A	GRCh38
NC_000001.10:g.983698T>A , CM000663.1:g.983698T>A	GRCh37
NC_000001.9:g.973561T>A	NCBI36
NG_016346.1:g.33196T>A , LRG_198:g.33196T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.4058T>A MANE Select	ENSP00000368678.2:p.Phe1353Tyr
ENST00000651234.1:c.3743T>A	ENSP00000499046.1:p.Phe1248Tyr
ENST00000652369.1:c.3743T>A	ENSP00000498543.1:p.Phe1248Tyr
ENST00000379370.6:c.4058T>A	ENSP00000368678.2:p.Phe1353Tyr
ENST00000620552.4:c.3644T>A	ENSP00000484607.1:p.Phe1215Tyr
NM_001305275.1:c.4058T>A	NP_001292204.1:p.Phe1353Tyr
NM_198576.3:c.4058T>A	NP_940978.2:p.Phe1353Tyr
XM_005244749.2:c.4058T>A	XP_005244806.1:p.Phe1353Tyr
XM_006710635.2:c.4058T>A	XP_006710698.1:p.Phe1353Tyr
XM_011541429.1:c.4058T>A	XP_011539731.1:p.Phe1353Tyr
XM_011541430.1:c.3185T>A	XP_011539732.1:p.Phe1062Tyr
XM_011541431.1:c.2324T>A	XP_011539733.1:p.Phe775Tyr
XR_946650.1:n.4125T>A
NM_001364727.1:c.3743T>A	NP_001351656.1:p.Phe1248Tyr
XM_005244749.3:c.4058T>A	XP_005244806.1:p.Phe1353Tyr
XM_011541429.2:c.4058T>A	XP_011539731.1:p.Phe1353Tyr
XR_946650.2:n.4129T>A
NM_001305275.2:c.4058T>A	NP_001292204.1:p.Phe1353Tyr
NM_198576.4:c.4058T>A MANE Select	NP_940978.2:p.Phe1353Tyr
NM_001364727.2:c.3743T>A	NP_001351656.1:p.Phe1248Tyr