Canonical Allele Identifier: CA1140572879

Gene: AGRN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1047818_1047819delinsGG , CM000663.2:g.1047818_1047819delinsGG	GRCh38
NC_000001.10:g.983198_983199delinsGG , CM000663.1:g.983198_983199delinsGG	GRCh37
NC_000001.9:g.973061_973062delinsGG	NCBI36
NG_016346.1:g.32696_32697delinsGG , LRG_198:g.32696_32697delinsGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.3674_3675delinsGG MANE Select	ENSP00000368678.2:p.Arg1225=
ENST00000651234.1:c.3359_3360delinsGG	ENSP00000499046.1:p.Arg1120=
ENST00000652369.1:c.3359_3360delinsGG	ENSP00000498543.1:p.Arg1120=
ENST00000379370.6:c.3674_3675delinsGG	ENSP00000368678.2:p.Arg1225=
ENST00000466223.1:n.412_413delinsGG
ENST00000478677.1:n.256_257delinsGG
ENST00000620552.4:c.3260_3261delinsGG	ENSP00000484607.1:p.Arg1087=
NM_001305275.1:c.3674_3675delinsGG	NP_001292204.1:p.Arg1225=
NM_198576.3:c.3674_3675delinsGG	NP_940978.2:p.Arg1225=
XM_005244749.2:c.3674_3675delinsGG	XP_005244806.1:p.Arg1225=
XM_006710635.2:c.3674_3675delinsGG	XP_006710698.1:p.Arg1225=
XM_011541429.1:c.3674_3675delinsGG	XP_011539731.1:p.Arg1225=
XM_011541430.1:c.2801_2802delinsGG	XP_011539732.1:p.Arg934=
XM_011541431.1:c.1940_1941delinsGG	XP_011539733.1:p.Arg647=
XR_946650.1:n.3741_3742delinsGG
NM_001364727.1:c.3359_3360delinsGG	NP_001351656.1:p.Arg1120=
XM_005244749.3:c.3674_3675delinsGG	XP_005244806.1:p.Arg1225=
XM_011541429.2:c.3674_3675delinsGG	XP_011539731.1:p.Arg1225=
XR_946650.2:n.3745_3746delinsGG
NM_001305275.2:c.3674_3675delinsGG	NP_001292204.1:p.Arg1225=
NM_198576.4:c.3674_3675delinsGG MANE Select	NP_940978.2:p.Arg1225=
NM_001364727.2:c.3359_3360delinsGG	NP_001351656.1:p.Arg1120=