Canonical Allele Identifier: CA1148801099

Gene: AGRN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1047728_1047729delinsTG , CM000663.2:g.1047728_1047729delinsTG	GRCh38
NC_000001.10:g.983108_983109delinsTG , CM000663.1:g.983108_983109delinsTG	GRCh37
NC_000001.9:g.972971_972972delinsTG	NCBI36
NG_016346.1:g.32606_32607delinsTG , LRG_198:g.32606_32607delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.3631+41_3631+42delinsTG MANE Select	ENSP00000368678.2:n.3631+41_3631+42delinsTG
ENST00000651234.1:c.3316+41_3316+42delinsTG	ENSP00000499046.1:n.3316+41_3316+42delinsTG
ENST00000652369.1:c.3316+41_3316+42delinsTG	ENSP00000498543.1:n.3316+41_3316+42delinsTG
ENST00000379370.6:c.3631+41_3631+42delinsTG	ENSP00000368678.2:n.3631+41_3631+42delinsTG
ENST00000466223.1:n.369+41_369+42delinsTG
ENST00000478677.1:n.213+41_213+42delinsTG
ENST00000620552.4:c.3217+41_3217+42delinsTG	ENSP00000484607.1:n.3217+41_3217+42delinsTG
NM_001305275.1:c.3631+41_3631+42delinsTG	NP_001292204.1:n.3631+41_3631+42delinsTG
NM_198576.3:c.3631+41_3631+42delinsTG	NP_940978.2:n.3631+41_3631+42delinsTG
XM_005244749.2:c.3631+41_3631+42delinsTG	XP_005244806.1:n.3631+41_3631+42delinsTG
XM_006710635.2:c.3631+41_3631+42delinsTG	XP_006710698.1:n.3631+41_3631+42delinsTG
XM_011541429.1:c.3631+41_3631+42delinsTG	XP_011539731.1:n.3631+41_3631+42delinsTG
XM_011541430.1:c.2758+41_2758+42delinsTG	XP_011539732.1:n.2758+41_2758+42delinsTG
XM_011541431.1:c.1897+41_1897+42delinsTG	XP_011539733.1:n.1897+41_1897+42delinsTG
XR_946650.1:n.3698+41_3698+42delinsTG
NM_001364727.1:c.3316+41_3316+42delinsTG	NP_001351656.1:n.3316+41_3316+42delinsTG
XM_005244749.3:c.3631+41_3631+42delinsTG	XP_005244806.1:n.3631+41_3631+42delinsTG
XM_011541429.2:c.3631+41_3631+42delinsTG	XP_011539731.1:n.3631+41_3631+42delinsTG
XR_946650.2:n.3702+41_3702+42delinsTG
NM_001305275.2:c.3631+41_3631+42delinsTG	NP_001292204.1:n.3631+41_3631+42delinsTG
NM_198576.4:c.3631+41_3631+42delinsTG MANE Select	NP_940978.2:n.3631+41_3631+42delinsTG
NM_001364727.2:c.3316+41_3316+42delinsTG	NP_001351656.1:n.3316+41_3316+42delinsTG