Canonical Allele Identifier: CA1144095920

Gene: AGRN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1047698C= , CM000663.2:g.1047698C=	GRCh38
NC_000001.10:g.983078C= , CM000663.1:g.983078C=	GRCh37
NC_000001.9:g.972941C=	NCBI36
NG_016346.1:g.32576C= , LRG_198:g.32576C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.3631+11C= MANE Select	ENSP00000368678.2:n.3631+11C=
ENST00000651234.1:c.3316+11C=	ENSP00000499046.1:n.3316+11C=
ENST00000652369.1:c.3316+11C=	ENSP00000498543.1:n.3316+11C=
ENST00000379370.6:c.3631+11C=	ENSP00000368678.2:n.3631+11C=
ENST00000466223.1:n.369+11C=
ENST00000478677.1:n.213+11C=
ENST00000620552.4:c.3217+11C=	ENSP00000484607.1:n.3217+11C=
NM_001305275.1:c.3631+11C=	NP_001292204.1:n.3631+11C=
NM_198576.3:c.3631+11C=	NP_940978.2:n.3631+11C=
XM_005244749.2:c.3631+11C=	XP_005244806.1:n.3631+11C=
XM_006710635.2:c.3631+11C=	XP_006710698.1:n.3631+11C=
XM_011541429.1:c.3631+11C=	XP_011539731.1:n.3631+11C=
XM_011541430.1:c.2758+11C=	XP_011539732.1:n.2758+11C=
XM_011541431.1:c.1897+11C=	XP_011539733.1:n.1897+11C=
XR_946650.1:n.3698+11C=
NM_001364727.1:c.3316+11C=	NP_001351656.1:n.3316+11C=
XM_005244749.3:c.3631+11C=	XP_005244806.1:n.3631+11C=
XM_011541429.2:c.3631+11C=	XP_011539731.1:n.3631+11C=
XR_946650.2:n.3702+11C=
NM_001305275.2:c.3631+11C=	NP_001292204.1:n.3631+11C=
NM_198576.4:c.3631+11C= MANE Select	NP_940978.2:n.3631+11C=
NM_001364727.2:c.3316+11C=	NP_001351656.1:n.3316+11C=