Canonical Allele Identifier: CA337779659

Gene: AGRN

Linked Data

• MyVariant Identifiers: chr1:g.985640T>A (hg19) ; chr1:g.1050260T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1050260T>A , CM000663.2:g.1050260T>A	GRCh38
NC_000001.10:g.985640T>A , CM000663.1:g.985640T>A	GRCh37
NC_000001.9:g.975503T>A	NCBI36
NG_016346.1:g.35138T>A , LRG_198:g.35138T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.4907T>A MANE Select	ENSP00000368678.2:p.Phe1636Tyr
ENST00000651234.1:c.4592T>A	ENSP00000499046.1:p.Phe1531Tyr
ENST00000652369.1:c.4592T>A	ENSP00000498543.1:p.Phe1531Tyr
ENST00000379370.6:c.4907T>A	ENSP00000368678.2:p.Phe1636Tyr
ENST00000620552.4:c.4493T>A	ENSP00000484607.1:p.Phe1498Tyr
NM_001305275.1:c.4907T>A	NP_001292204.1:p.Phe1636Tyr
NM_198576.3:c.4907T>A	NP_940978.2:p.Phe1636Tyr
XM_005244749.2:c.4907T>A	XP_005244806.1:p.Phe1636Tyr
XM_006710635.2:c.4907T>A	XP_006710698.1:p.Phe1636Tyr
XM_011541429.1:c.4907T>A	XP_011539731.1:p.Phe1636Tyr
XM_011541430.1:c.4034T>A	XP_011539732.1:p.Phe1345Tyr
XM_011541431.1:c.3173T>A	XP_011539733.1:p.Phe1058Tyr
XR_946650.1:n.4974T>A
NM_001364727.1:c.4592T>A	NP_001351656.1:p.Phe1531Tyr
XM_005244749.3:c.4907T>A	XP_005244806.1:p.Phe1636Tyr
XM_011541429.2:c.4907T>A	XP_011539731.1:p.Phe1636Tyr
XR_946650.2:n.4978T>A
NM_001305275.2:c.4907T>A	NP_001292204.1:p.Phe1636Tyr
NM_198576.4:c.4907T>A MANE Select	NP_940978.2:p.Phe1636Tyr
NM_001364727.2:c.4592T>A	NP_001351656.1:p.Phe1531Tyr