Canonical Allele Identifier: CA337853235

Gene: AGRN

Linked Data

• dbSNP Id: rs1553177224
• MyVariant Identifiers: chr1:g.983623_983624insCT (hg19) ; chr1:g.1048243_1048244insCT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1048243_1048244insCT , CM000663.2:g.1048243_1048244insCT	GRCh38
NC_000001.10:g.983623_983624insCT , CM000663.1:g.983623_983624insCT	GRCh37
NC_000001.9:g.973486_973487insCT	NCBI36
NG_016346.1:g.33121_33122insCT , LRG_198:g.33121_33122insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.3983_3984insCT MANE Select	ENSP00000368678.2:p.Gln1328HisfsTer?
ENST00000651234.1:c.3668_3669insCT	ENSP00000499046.1:p.Gln1223HisfsTer?
ENST00000652369.1:c.3668_3669insCT	ENSP00000498543.1:p.Gln1223HisfsTer?
ENST00000379370.6:c.3983_3984insCT	ENSP00000368678.2:p.Gln1328HisfsTer?
ENST00000620552.4:c.3569_3570insCT	ENSP00000484607.1:p.Gln1190HisfsTer?
NM_001305275.1:c.3983_3984insCT	NP_001292204.1:p.Gln1328HisfsTer?
NM_198576.3:c.3983_3984insCT	NP_940978.2:p.Gln1328HisfsTer?
XM_005244749.2:c.3983_3984insCT	XP_005244806.1:p.Gln1328HisfsTer?
XM_006710635.2:c.3983_3984insCT	XP_006710698.1:p.Gln1328HisfsTer?
XM_011541429.1:c.3983_3984insCT	XP_011539731.1:p.Gln1328HisfsTer?
XM_011541430.1:c.3110_3111insCT	XP_011539732.1:p.Gln1037HisfsTer?
XM_011541431.1:c.2249_2250insCT	XP_011539733.1:p.Gln750HisfsTer?
XR_946650.1:n.4050_4051insCT
NM_001364727.1:c.3668_3669insCT	NP_001351656.1:p.Gln1223HisfsTer?
XM_005244749.3:c.3983_3984insCT	XP_005244806.1:p.Gln1328HisfsTer?
XM_011541429.2:c.3983_3984insCT	XP_011539731.1:p.Gln1328HisfsTer?
XR_946650.2:n.4054_4055insCT
NM_001305275.2:c.3983_3984insCT	NP_001292204.1:p.Gln1328HisfsTer?
NM_198576.4:c.3983_3984insCT MANE Select	NP_940978.2:p.Gln1328HisfsTer?
NM_001364727.2:c.3668_3669insCT	NP_001351656.1:p.Gln1223HisfsTer?