Canonical Allele Identifier: CA337779141

Gene: AGRN

Linked Data

• MyVariant Identifiers: chr1:g.985137C>G (hg19) ; chr1:g.1049757C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1049757C>G , CM000663.2:g.1049757C>G	GRCh38
NC_000001.10:g.985137C>G , CM000663.1:g.985137C>G	GRCh37
NC_000001.9:g.975000C>G	NCBI36
NG_016346.1:g.34635C>G , LRG_198:g.34635C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.4706C>G MANE Select	ENSP00000368678.2:p.Ala1569Gly
ENST00000651234.1:c.4391C>G	ENSP00000499046.1:p.Ala1464Gly
ENST00000652369.1:c.4391C>G	ENSP00000498543.1:p.Ala1464Gly
ENST00000379370.6:c.4706C>G	ENSP00000368678.2:p.Ala1569Gly
ENST00000620552.4:c.4292C>G	ENSP00000484607.1:p.Ala1431Gly
NM_001305275.1:c.4706C>G	NP_001292204.1:p.Ala1569Gly
NM_198576.3:c.4706C>G	NP_940978.2:p.Ala1569Gly
XM_005244749.2:c.4706C>G	XP_005244806.1:p.Ala1569Gly
XM_006710635.2:c.4706C>G	XP_006710698.1:p.Ala1569Gly
XM_011541429.1:c.4706C>G	XP_011539731.1:p.Ala1569Gly
XM_011541430.1:c.3833C>G	XP_011539732.1:p.Ala1278Gly
XM_011541431.1:c.2972C>G	XP_011539733.1:p.Ala991Gly
XR_946650.1:n.4773C>G
NM_001364727.1:c.4391C>G	NP_001351656.1:p.Ala1464Gly
XM_005244749.3:c.4706C>G	XP_005244806.1:p.Ala1569Gly
XM_011541429.2:c.4706C>G	XP_011539731.1:p.Ala1569Gly
XR_946650.2:n.4777C>G
NM_001305275.2:c.4706C>G	NP_001292204.1:p.Ala1569Gly
NM_198576.4:c.4706C>G MANE Select	NP_940978.2:p.Ala1569Gly
NM_001364727.2:c.4391C>G	NP_001351656.1:p.Ala1464Gly