Canonical Allele Identifier: CA508395

Gene: AGRN

Linked Data

• dbSNP Id: rs770946661
• ExAC: 1:979372 C / G
• gnomAD v2: 1-979372-C-G
• gnomAD v4: 1-1043992-C-G
• MyVariant Identifiers: chr1:g.979372C>G (hg19) ; chr1:g.1043992C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1043992C>G , CM000663.2:g.1043992C>G	GRCh38
NC_000001.10:g.979372C>G , CM000663.1:g.979372C>G	GRCh37
NC_000001.9:g.969235C>G	NCBI36
NG_016346.1:g.28870C>G , LRG_198:g.28870C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.1968C>G MANE Select	ENSP00000368678.2:p.Ile656Met
ENST00000651234.1:c.1653C>G	ENSP00000499046.1:p.Ile551Met
ENST00000652369.1:c.1653C>G	ENSP00000498543.1:p.Ile551Met
ENST00000379370.6:c.1968C>G	ENSP00000368678.2:p.Ile656Met
ENST00000620552.4:c.1554C>G	ENSP00000484607.1:p.Ile518Met
NM_001305275.1:c.1968C>G	NP_001292204.1:p.Ile656Met
NM_198576.3:c.1968C>G	NP_940978.2:p.Ile656Met
XM_005244749.2:c.1968C>G	XP_005244806.1:p.Ile656Met
XM_006710635.2:c.1968C>G	XP_006710698.1:p.Ile656Met
XM_011541429.1:c.1968C>G	XP_011539731.1:p.Ile656Met
XM_011541430.1:c.1095C>G	XP_011539732.1:p.Ile365Met
XM_011541431.1:c.234C>G	XP_011539733.1:p.Ile78Met
XR_946650.1:n.2035C>G
NM_001364727.1:c.1653C>G	NP_001351656.1:p.Ile551Met
XM_005244749.3:c.1968C>G	XP_005244806.1:p.Ile656Met
XM_011541429.2:c.1968C>G	XP_011539731.1:p.Ile656Met
XR_946650.2:n.2039C>G
NM_001305275.2:c.1968C>G	NP_001292204.1:p.Ile656Met
NM_198576.4:c.1968C>G MANE Select	NP_940978.2:p.Ile656Met
NM_001364727.2:c.1653C>G	NP_001351656.1:p.Ile551Met