Canonical Allele Identifier: CA1148773906

Gene: AGRN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1044062G= , CM000663.2:g.1044062G=	GRCh38
NC_000001.10:g.979442G= , CM000663.1:g.979442G=	GRCh37
NC_000001.9:g.969305G=	NCBI36
NG_016346.1:g.28940G= , LRG_198:g.28940G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.1999+39G= MANE Select	ENSP00000368678.2:n.1999+39G=
ENST00000651234.1:c.1684+39G=	ENSP00000499046.1:n.1684+39G=
ENST00000652369.1:c.1684+39G=	ENSP00000498543.1:n.1684+39G=
ENST00000379370.6:c.1999+39G=	ENSP00000368678.2:n.1999+39G=
ENST00000620552.4:c.1585+39G=	ENSP00000484607.1:n.1585+39G=
NM_001305275.1:c.1999+39G=	NP_001292204.1:n.1999+39G=
NM_198576.3:c.1999+39G=	NP_940978.2:n.1999+39G=
XM_005244749.2:c.1999+39G=	XP_005244806.1:n.1999+39G=
XM_006710635.2:c.1999+39G=	XP_006710698.1:n.1999+39G=
XM_011541429.1:c.1999+39G=	XP_011539731.1:n.1999+39G=
XM_011541430.1:c.1126+39G=	XP_011539732.1:n.1126+39G=
XM_011541431.1:c.265+39G=	XP_011539733.1:n.265+39G=
XR_946650.1:n.2066+39G=
NM_001364727.1:c.1684+39G=	NP_001351656.1:n.1684+39G=
XM_005244749.3:c.1999+39G=	XP_005244806.1:n.1999+39G=
XM_011541429.2:c.1999+39G=	XP_011539731.1:n.1999+39G=
XR_946650.2:n.2070+39G=
NM_001305275.2:c.1999+39G=	NP_001292204.1:n.1999+39G=
NM_198576.4:c.1999+39G= MANE Select	NP_940978.2:n.1999+39G=
NM_001364727.2:c.1684+39G=	NP_001351656.1:n.1684+39G=