Canonical Allele Identifier: CA1144301476

Gene: AGRN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1047829G= , CM000663.2:g.1047829G=	GRCh38
NC_000001.10:g.983209G= , CM000663.1:g.983209G=	GRCh37
NC_000001.9:g.973072G=	NCBI36
NG_016346.1:g.32707G= , LRG_198:g.32707G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.3685G= MANE Select	ENSP00000368678.2:p.Val1229=
ENST00000651234.1:c.3370G=	ENSP00000499046.1:p.Val1124=
ENST00000652369.1:c.3370G=	ENSP00000498543.1:p.Val1124=
ENST00000379370.6:c.3685G=	ENSP00000368678.2:p.Val1229=
ENST00000466223.1:n.423G=
ENST00000478677.1:n.267G=
ENST00000620552.4:c.3271G=	ENSP00000484607.1:p.Val1091=
NM_001305275.1:c.3685G=	NP_001292204.1:p.Val1229=
NM_198576.3:c.3685G=	NP_940978.2:p.Val1229=
XM_005244749.2:c.3685G=	XP_005244806.1:p.Val1229=
XM_006710635.2:c.3685G=	XP_006710698.1:p.Val1229=
XM_011541429.1:c.3685G=	XP_011539731.1:p.Val1229=
XM_011541430.1:c.2812G=	XP_011539732.1:p.Val938=
XM_011541431.1:c.1951G=	XP_011539733.1:p.Val651=
XR_946650.1:n.3752G=
NM_001364727.1:c.3370G=	NP_001351656.1:p.Val1124=
XM_005244749.3:c.3685G=	XP_005244806.1:p.Val1229=
XM_011541429.2:c.3685G=	XP_011539731.1:p.Val1229=
XR_946650.2:n.3756G=
NM_001305275.2:c.3685G=	NP_001292204.1:p.Val1229=
NM_198576.4:c.3685G= MANE Select	NP_940978.2:p.Val1229=
NM_001364727.2:c.3370G=	NP_001351656.1:p.Val1124=