Canonical Allele Identifier: CA415758322

Gene: AGRN

Linked Data

• dbSNP Id: rs746943998
• MyVariant Identifiers: chr1:g.983564T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1048184T>A , CM000663.2:g.1048184T>A	GRCh38
NC_000001.10:g.983564T>A , CM000663.1:g.983564T>A	GRCh37
NC_000001.9:g.973427T>A	NCBI36
NG_016346.1:g.33062T>A , LRG_198:g.33062T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.3924T>A MANE Select	ENSP00000368678.2:p.Arg1308=
ENST00000651234.1:c.3609T>A	ENSP00000499046.1:p.Arg1203=
ENST00000652369.1:c.3609T>A	ENSP00000498543.1:p.Arg1203=
ENST00000379370.6:c.3924T>A	ENSP00000368678.2:p.Arg1308=
ENST00000620552.4:c.3510T>A	ENSP00000484607.1:p.Arg1170=
NM_001305275.1:c.3924T>A	NP_001292204.1:p.Arg1308=
NM_198576.3:c.3924T>A	NP_940978.2:p.Arg1308=
XM_005244749.2:c.3924T>A	XP_005244806.1:p.Arg1308=
XM_006710635.2:c.3924T>A	XP_006710698.1:p.Arg1308=
XM_011541429.1:c.3924T>A	XP_011539731.1:p.Arg1308=
XM_011541430.1:c.3051T>A	XP_011539732.1:p.Arg1017=
XM_011541431.1:c.2190T>A	XP_011539733.1:p.Arg730=
XR_946650.1:n.3991T>A
NM_001364727.1:c.3609T>A	NP_001351656.1:p.Arg1203=
XM_005244749.3:c.3924T>A	XP_005244806.1:p.Arg1308=
XM_011541429.2:c.3924T>A	XP_011539731.1:p.Arg1308=
XR_946650.2:n.3995T>A
NM_001305275.2:c.3924T>A	NP_001292204.1:p.Arg1308=
NM_198576.4:c.3924T>A MANE Select	NP_940978.2:p.Arg1308=
NM_001364727.2:c.3609T>A	NP_001351656.1:p.Arg1203=