Canonical Allele Identifier: CA1146656663

Gene: AGRN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1047825C= , CM000663.2:g.1047825C=	GRCh38
NC_000001.10:g.983205C= , CM000663.1:g.983205C=	GRCh37
NC_000001.9:g.973068C=	NCBI36
NG_016346.1:g.32703C= , LRG_198:g.32703C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.3681C= MANE Select	ENSP00000368678.2:p.Ile1227=
ENST00000651234.1:c.3366C=	ENSP00000499046.1:p.Ile1122=
ENST00000652369.1:c.3366C=	ENSP00000498543.1:p.Ile1122=
ENST00000379370.6:c.3681C=	ENSP00000368678.2:p.Ile1227=
ENST00000466223.1:n.419C=
ENST00000478677.1:n.263C=
ENST00000620552.4:c.3267C=	ENSP00000484607.1:p.Ile1089=
NM_001305275.1:c.3681C=	NP_001292204.1:p.Ile1227=
NM_198576.3:c.3681C=	NP_940978.2:p.Ile1227=
XM_005244749.2:c.3681C=	XP_005244806.1:p.Ile1227=
XM_006710635.2:c.3681C=	XP_006710698.1:p.Ile1227=
XM_011541429.1:c.3681C=	XP_011539731.1:p.Ile1227=
XM_011541430.1:c.2808C=	XP_011539732.1:p.Ile936=
XM_011541431.1:c.1947C=	XP_011539733.1:p.Ile649=
XR_946650.1:n.3748C=
NM_001364727.1:c.3366C=	NP_001351656.1:p.Ile1122=
XM_005244749.3:c.3681C=	XP_005244806.1:p.Ile1227=
XM_011541429.2:c.3681C=	XP_011539731.1:p.Ile1227=
XR_946650.2:n.3752C=
NM_001305275.2:c.3681C=	NP_001292204.1:p.Ile1227=
NM_198576.4:c.3681C= MANE Select	NP_940978.2:p.Ile1227=
NM_001364727.2:c.3366C=	NP_001351656.1:p.Ile1122=