Canonical Allele Identifier: CA415757224

Gene: AGRN

Linked Data

• MyVariant Identifiers: chr1:g.979559C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1044179C>G , CM000663.2:g.1044179C>G	GRCh38
NC_000001.10:g.979559C>G , CM000663.1:g.979559C>G	GRCh37
NC_000001.9:g.969422C>G	NCBI36
NG_016346.1:g.29057C>G , LRG_198:g.29057C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.2070C>G MANE Select	ENSP00000368678.2:p.Arg690=
ENST00000651234.1:c.1755C>G	ENSP00000499046.1:p.Arg585=
ENST00000652369.1:c.1755C>G	ENSP00000498543.1:p.Arg585=
ENST00000379370.6:c.2070C>G	ENSP00000368678.2:p.Arg690=
ENST00000620552.4:c.1656C>G	ENSP00000484607.1:p.Arg552=
NM_001305275.1:c.2070C>G	NP_001292204.1:p.Arg690=
NM_198576.3:c.2070C>G	NP_940978.2:p.Arg690=
XM_005244749.2:c.2070C>G	XP_005244806.1:p.Arg690=
XM_006710635.2:c.2070C>G	XP_006710698.1:p.Arg690=
XM_011541429.1:c.2070C>G	XP_011539731.1:p.Arg690=
XM_011541430.1:c.1197C>G	XP_011539732.1:p.Arg399=
XM_011541431.1:c.336C>G	XP_011539733.1:p.Arg112=
XR_946650.1:n.2137C>G
NM_001364727.1:c.1755C>G	NP_001351656.1:p.Arg585=
XM_005244749.3:c.2070C>G	XP_005244806.1:p.Arg690=
XM_011541429.2:c.2070C>G	XP_011539731.1:p.Arg690=
XR_946650.2:n.2141C>G
NM_001305275.2:c.2070C>G	NP_001292204.1:p.Arg690=
NM_198576.4:c.2070C>G MANE Select	NP_940978.2:p.Arg690=
NM_001364727.2:c.1755C>G	NP_001351656.1:p.Arg585=