Canonical Allele Identifier: CA1148747567

Gene: AGRN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1049945C= , CM000663.2:g.1049945C=	GRCh38
NC_000001.10:g.985325C= , CM000663.1:g.985325C=	GRCh37
NC_000001.9:g.975188C=	NCBI36
NG_016346.1:g.34823C= , LRG_198:g.34823C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.4787C= MANE Select	ENSP00000368678.2:p.Pro1596=
ENST00000651234.1:c.4472C=	ENSP00000499046.1:p.Pro1491=
ENST00000652369.1:c.4472C=	ENSP00000498543.1:p.Pro1491=
ENST00000379370.6:c.4787C=	ENSP00000368678.2:p.Pro1596=
ENST00000620552.4:c.4373C=	ENSP00000484607.1:p.Pro1458=
NM_001305275.1:c.4787C=	NP_001292204.1:p.Pro1596=
NM_198576.3:c.4787C=	NP_940978.2:p.Pro1596=
XM_005244749.2:c.4787C=	XP_005244806.1:p.Pro1596=
XM_006710635.2:c.4787C=	XP_006710698.1:p.Pro1596=
XM_011541429.1:c.4787C=	XP_011539731.1:p.Pro1596=
XM_011541430.1:c.3914C=	XP_011539732.1:p.Pro1305=
XM_011541431.1:c.3053C=	XP_011539733.1:p.Pro1018=
XR_946650.1:n.4854C=
NM_001364727.1:c.4472C=	NP_001351656.1:p.Pro1491=
XM_005244749.3:c.4787C=	XP_005244806.1:p.Pro1596=
XM_011541429.2:c.4787C=	XP_011539731.1:p.Pro1596=
XR_946650.2:n.4858C=
NM_001305275.2:c.4787C=	NP_001292204.1:p.Pro1596=
NM_198576.4:c.4787C= MANE Select	NP_940978.2:p.Pro1596=
NM_001364727.2:c.4472C=	NP_001351656.1:p.Pro1491=