Canonical Allele Identifier: CA508439

Gene: AGRN

Linked Data

• dbSNP Id: rs141603403
• ExAC: 1:979502 C / G
• gnomAD v2: 1-979502-C-G
• gnomAD v4: 1-1044122-C-G
• MyVariant Identifiers: chr1:g.979502C>G (hg19) ; chr1:g.1044122C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1044122C>G , CM000663.2:g.1044122C>G	GRCh38
NC_000001.10:g.979502C>G , CM000663.1:g.979502C>G	GRCh37
NC_000001.9:g.969365C>G	NCBI36
NG_016346.1:g.29000C>G , LRG_198:g.29000C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.2013C>G MANE Select	ENSP00000368678.2:p.Ser671=
ENST00000651234.1:c.1698C>G	ENSP00000499046.1:p.Ser566=
ENST00000652369.1:c.1698C>G	ENSP00000498543.1:p.Ser566=
ENST00000379370.6:c.2013C>G	ENSP00000368678.2:p.Ser671=
ENST00000620552.4:c.1599C>G	ENSP00000484607.1:p.Ser533=
NM_001305275.1:c.2013C>G	NP_001292204.1:p.Ser671=
NM_198576.3:c.2013C>G	NP_940978.2:p.Ser671=
XM_005244749.2:c.2013C>G	XP_005244806.1:p.Ser671=
XM_006710635.2:c.2013C>G	XP_006710698.1:p.Ser671=
XM_011541429.1:c.2013C>G	XP_011539731.1:p.Ser671=
XM_011541430.1:c.1140C>G	XP_011539732.1:p.Ser380=
XM_011541431.1:c.279C>G	XP_011539733.1:p.Ser93=
XR_946650.1:n.2080C>G
NM_001364727.1:c.1698C>G	NP_001351656.1:p.Ser566=
XM_005244749.3:c.2013C>G	XP_005244806.1:p.Ser671=
XM_011541429.2:c.2013C>G	XP_011539731.1:p.Ser671=
XR_946650.2:n.2084C>G
NM_001305275.2:c.2013C>G	NP_001292204.1:p.Ser671=
NM_198576.4:c.2013C>G MANE Select	NP_940978.2:p.Ser671=
NM_001364727.2:c.1698C>G	NP_001351656.1:p.Ser566=