Canonical Allele Identifier: CA1142308223

Gene: AGRN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1049979C= , CM000663.2:g.1049979C=	GRCh38
NC_000001.10:g.985359C= , CM000663.1:g.985359C=	GRCh37
NC_000001.9:g.975222C=	NCBI36
NG_016346.1:g.34857C= , LRG_198:g.34857C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.4821C= MANE Select	ENSP00000368678.2:p.Pro1607=
ENST00000651234.1:c.4506C=	ENSP00000499046.1:p.Pro1502=
ENST00000652369.1:c.4506C=	ENSP00000498543.1:p.Pro1502=
ENST00000379370.6:c.4821C=	ENSP00000368678.2:p.Pro1607=
ENST00000620552.4:c.4407C=	ENSP00000484607.1:p.Pro1469=
NM_001305275.1:c.4821C=	NP_001292204.1:p.Pro1607=
NM_198576.3:c.4821C=	NP_940978.2:p.Pro1607=
XM_005244749.2:c.4821C=	XP_005244806.1:p.Pro1607=
XM_006710635.2:c.4821C=	XP_006710698.1:p.Pro1607=
XM_011541429.1:c.4821C=	XP_011539731.1:p.Pro1607=
XM_011541430.1:c.3948C=	XP_011539732.1:p.Pro1316=
XM_011541431.1:c.3087C=	XP_011539733.1:p.Pro1029=
XR_946650.1:n.4888C=
NM_001364727.1:c.4506C=	NP_001351656.1:p.Pro1502=
XM_005244749.3:c.4821C=	XP_005244806.1:p.Pro1607=
XM_011541429.2:c.4821C=	XP_011539731.1:p.Pro1607=
XR_946650.2:n.4892C=
NM_001305275.2:c.4821C=	NP_001292204.1:p.Pro1607=
NM_198576.4:c.4821C= MANE Select	NP_940978.2:p.Pro1607=
NM_001364727.2:c.4506C=	NP_001351656.1:p.Pro1502=