Canonical Allele Identifier: CA415758428

Gene: AGRN

Linked Data

• MyVariant Identifiers: chr1:g.983615C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1048235C>G , CM000663.2:g.1048235C>G	GRCh38
NC_000001.10:g.983615C>G , CM000663.1:g.983615C>G	GRCh37
NC_000001.9:g.973478C>G	NCBI36
NG_016346.1:g.33113C>G , LRG_198:g.33113C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.3975C>G MANE Select	ENSP00000368678.2:p.Ala1325=
ENST00000651234.1:c.3660C>G	ENSP00000499046.1:p.Ala1220=
ENST00000652369.1:c.3660C>G	ENSP00000498543.1:p.Ala1220=
ENST00000379370.6:c.3975C>G	ENSP00000368678.2:p.Ala1325=
ENST00000620552.4:c.3561C>G	ENSP00000484607.1:p.Ala1187=
NM_001305275.1:c.3975C>G	NP_001292204.1:p.Ala1325=
NM_198576.3:c.3975C>G	NP_940978.2:p.Ala1325=
XM_005244749.2:c.3975C>G	XP_005244806.1:p.Ala1325=
XM_006710635.2:c.3975C>G	XP_006710698.1:p.Ala1325=
XM_011541429.1:c.3975C>G	XP_011539731.1:p.Ala1325=
XM_011541430.1:c.3102C>G	XP_011539732.1:p.Ala1034=
XM_011541431.1:c.2241C>G	XP_011539733.1:p.Ala747=
XR_946650.1:n.4042C>G
NM_001364727.1:c.3660C>G	NP_001351656.1:p.Ala1220=
XM_005244749.3:c.3975C>G	XP_005244806.1:p.Ala1325=
XM_011541429.2:c.3975C>G	XP_011539731.1:p.Ala1325=
XR_946650.2:n.4046C>G
NM_001305275.2:c.3975C>G	NP_001292204.1:p.Ala1325=
NM_198576.4:c.3975C>G MANE Select	NP_940978.2:p.Ala1325=
NM_001364727.2:c.3660C>G	NP_001351656.1:p.Ala1220=