Canonical Allele Identifier: CA509142

Gene: AGRN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1047624C>A , CM000663.2:g.1047624C>A	GRCh38
NC_000001.10:g.983004C>A , CM000663.1:g.983004C>A	GRCh37
NC_000001.9:g.972867C>A	NCBI36
NG_016346.1:g.32502C>A , LRG_198:g.32502C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.3568C>A MANE Select	ENSP00000368678.2:p.Arg1190Ser
ENST00000651234.1:c.3253C>A	ENSP00000499046.1:p.Arg1085Ser
ENST00000652369.1:c.3253C>A	ENSP00000498543.1:p.Arg1085Ser
ENST00000379370.6:c.3568C>A	ENSP00000368678.2:p.Arg1190Ser
ENST00000466223.1:n.306C>A
ENST00000478677.1:n.150C>A
ENST00000620552.4:c.3154C>A	ENSP00000484607.1:p.Arg1052Ser
NM_001305275.1:c.3568C>A	NP_001292204.1:p.Arg1190Ser
NM_198576.3:c.3568C>A	NP_940978.2:p.Arg1190Ser
XM_005244749.2:c.3568C>A	XP_005244806.1:p.Arg1190Ser
XM_006710635.2:c.3568C>A	XP_006710698.1:p.Arg1190Ser
XM_011541429.1:c.3568C>A	XP_011539731.1:p.Arg1190Ser
XM_011541430.1:c.2695C>A	XP_011539732.1:p.Arg899Ser
XM_011541431.1:c.1834C>A	XP_011539733.1:p.Arg612Ser
XR_946650.1:n.3635C>A
NM_001364727.1:c.3253C>A	NP_001351656.1:p.Arg1085Ser
XM_005244749.3:c.3568C>A	XP_005244806.1:p.Arg1190Ser
XM_011541429.2:c.3568C>A	XP_011539731.1:p.Arg1190Ser
XR_946650.2:n.3639C>A
NM_001305275.2:c.3568C>A	NP_001292204.1:p.Arg1190Ser
NM_198576.4:c.3568C>A MANE Select	NP_940978.2:p.Arg1190Ser
NM_001364727.2:c.3253C>A	NP_001351656.1:p.Arg1085Ser