Canonical Allele Identifier: CA337852228

Gene: AGRN

Linked Data

• MyVariant Identifiers: chr1:g.983411C>G (hg19) ; chr1:g.1048031C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1048031C>G , CM000663.2:g.1048031C>G	GRCh38
NC_000001.10:g.983411C>G , CM000663.1:g.983411C>G	GRCh37
NC_000001.9:g.973274C>G	NCBI36
NG_016346.1:g.32909C>G , LRG_198:g.32909C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.3771C>G MANE Select	ENSP00000368678.2:p.Ile1257Met
ENST00000651234.1:c.3456C>G	ENSP00000499046.1:p.Ile1152Met
ENST00000652369.1:c.3456C>G	ENSP00000498543.1:p.Ile1152Met
ENST00000379370.6:c.3771C>G	ENSP00000368678.2:p.Ile1257Met
ENST00000620552.4:c.3357C>G	ENSP00000484607.1:p.Ile1119Met
NM_001305275.1:c.3771C>G	NP_001292204.1:p.Ile1257Met
NM_198576.3:c.3771C>G	NP_940978.2:p.Ile1257Met
XM_005244749.2:c.3771C>G	XP_005244806.1:p.Ile1257Met
XM_006710635.2:c.3771C>G	XP_006710698.1:p.Ile1257Met
XM_011541429.1:c.3771C>G	XP_011539731.1:p.Ile1257Met
XM_011541430.1:c.2898C>G	XP_011539732.1:p.Ile966Met
XM_011541431.1:c.2037C>G	XP_011539733.1:p.Ile679Met
XR_946650.1:n.3838C>G
NM_001364727.1:c.3456C>G	NP_001351656.1:p.Ile1152Met
XM_005244749.3:c.3771C>G	XP_005244806.1:p.Ile1257Met
XM_011541429.2:c.3771C>G	XP_011539731.1:p.Ile1257Met
XR_946650.2:n.3842C>G
NM_001305275.2:c.3771C>G	NP_001292204.1:p.Ile1257Met
NM_198576.4:c.3771C>G MANE Select	NP_940978.2:p.Ile1257Met
NM_001364727.2:c.3456C>G	NP_001351656.1:p.Ile1152Met