Canonical Allele Identifier: CA1148713442

Gene: AGRN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1043840G= , CM000663.2:g.1043840G=	GRCh38
NC_000001.10:g.979220G= , CM000663.1:g.979220G=	GRCh37
NC_000001.9:g.969083G=	NCBI36
NG_016346.1:g.28718G= , LRG_198:g.28718G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.1816G= MANE Select	ENSP00000368678.2:p.Val606=
ENST00000651234.1:c.1501G=	ENSP00000499046.1:p.Val501=
ENST00000652369.1:c.1501G=	ENSP00000498543.1:p.Val501=
ENST00000379370.6:c.1816G=	ENSP00000368678.2:p.Val606=
ENST00000620552.4:c.1402G=	ENSP00000484607.1:p.Val468=
NM_001305275.1:c.1816G=	NP_001292204.1:p.Val606=
NM_198576.3:c.1816G=	NP_940978.2:p.Val606=
XM_005244749.2:c.1816G=	XP_005244806.1:p.Val606=
XM_006710635.2:c.1816G=	XP_006710698.1:p.Val606=
XM_011541429.1:c.1816G=	XP_011539731.1:p.Val606=
XM_011541430.1:c.943G=	XP_011539732.1:p.Val315=
XM_011541431.1:c.82G=	XP_011539733.1:p.Val28=
XR_946650.1:n.1883G=
NM_001364727.1:c.1501G=	NP_001351656.1:p.Val501=
XM_005244749.3:c.1816G=	XP_005244806.1:p.Val606=
XM_011541429.2:c.1816G=	XP_011539731.1:p.Val606=
XR_946650.2:n.1887G=
NM_001305275.2:c.1816G=	NP_001292204.1:p.Val606=
NM_198576.4:c.1816G= MANE Select	NP_940978.2:p.Val606=
NM_001364727.2:c.1501G=	NP_001351656.1:p.Val501=