Canonical Allele Identifier: CA337853404

Gene: AGRN

Linked Data

• dbSNP Id: rs867208955
• gnomAD v2: 1-983691-G-C
• gnomAD v3: 1-1048311-G-C
• gnomAD v4: 1-1048311-G-C
• MyVariant Identifiers: chr1:g.983691G>C (hg19) ; chr1:g.1048311G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1048311G>C , CM000663.2:g.1048311G>C	GRCh38
NC_000001.10:g.983691G>C , CM000663.1:g.983691G>C	GRCh37
NC_000001.9:g.973554G>C	NCBI36
NG_016346.1:g.33189G>C , LRG_198:g.33189G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.4051G>C MANE Select	ENSP00000368678.2:p.Gly1351Arg
ENST00000651234.1:c.3736G>C	ENSP00000499046.1:p.Gly1246Arg
ENST00000652369.1:c.3736G>C	ENSP00000498543.1:p.Gly1246Arg
ENST00000379370.6:c.4051G>C	ENSP00000368678.2:p.Gly1351Arg
ENST00000620552.4:c.3637G>C	ENSP00000484607.1:p.Gly1213Arg
NM_001305275.1:c.4051G>C	NP_001292204.1:p.Gly1351Arg
NM_198576.3:c.4051G>C	NP_940978.2:p.Gly1351Arg
XM_005244749.2:c.4051G>C	XP_005244806.1:p.Gly1351Arg
XM_006710635.2:c.4051G>C	XP_006710698.1:p.Gly1351Arg
XM_011541429.1:c.4051G>C	XP_011539731.1:p.Gly1351Arg
XM_011541430.1:c.3178G>C	XP_011539732.1:p.Gly1060Arg
XM_011541431.1:c.2317G>C	XP_011539733.1:p.Gly773Arg
XR_946650.1:n.4118G>C
NM_001364727.1:c.3736G>C	NP_001351656.1:p.Gly1246Arg
XM_005244749.3:c.4051G>C	XP_005244806.1:p.Gly1351Arg
XM_011541429.2:c.4051G>C	XP_011539731.1:p.Gly1351Arg
XR_946650.2:n.4122G>C
NM_001305275.2:c.4051G>C	NP_001292204.1:p.Gly1351Arg
NM_198576.4:c.4051G>C MANE Select	NP_940978.2:p.Gly1351Arg
NM_001364727.2:c.3736G>C	NP_001351656.1:p.Gly1246Arg