Canonical Allele Identifier: CA337779685

Gene: AGRN

Linked Data

• MyVariant Identifiers: chr1:g.985652T>A (hg19) ; chr1:g.1050272T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1050272T>A , CM000663.2:g.1050272T>A	GRCh38
NC_000001.10:g.985652T>A , CM000663.1:g.985652T>A	GRCh37
NC_000001.9:g.975515T>A	NCBI36
NG_016346.1:g.35150T>A , LRG_198:g.35150T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.4919T>A MANE Select	ENSP00000368678.2:p.Phe1640Tyr
ENST00000651234.1:c.4604T>A	ENSP00000499046.1:p.Phe1535Tyr
ENST00000652369.1:c.4604T>A	ENSP00000498543.1:p.Phe1535Tyr
ENST00000379370.6:c.4919T>A	ENSP00000368678.2:p.Phe1640Tyr
ENST00000620552.4:c.4505T>A	ENSP00000484607.1:p.Phe1502Tyr
NM_001305275.1:c.4919T>A	NP_001292204.1:p.Phe1640Tyr
NM_198576.3:c.4919T>A	NP_940978.2:p.Phe1640Tyr
XM_005244749.2:c.4919T>A	XP_005244806.1:p.Phe1640Tyr
XM_006710635.2:c.4919T>A	XP_006710698.1:p.Phe1640Tyr
XM_011541429.1:c.4919T>A	XP_011539731.1:p.Phe1640Tyr
XM_011541430.1:c.4046T>A	XP_011539732.1:p.Phe1349Tyr
XM_011541431.1:c.3185T>A	XP_011539733.1:p.Phe1062Tyr
XR_946650.1:n.4986T>A
NM_001364727.1:c.4604T>A	NP_001351656.1:p.Phe1535Tyr
XM_005244749.3:c.4919T>A	XP_005244806.1:p.Phe1640Tyr
XM_011541429.2:c.4919T>A	XP_011539731.1:p.Phe1640Tyr
XR_946650.2:n.4990T>A
NM_001305275.2:c.4919T>A	NP_001292204.1:p.Phe1640Tyr
NM_198576.4:c.4919T>A MANE Select	NP_940978.2:p.Phe1640Tyr
NM_001364727.2:c.4604T>A	NP_001351656.1:p.Phe1535Tyr