Canonical Allele Identifier: CA337851270

Gene: AGRN

Linked Data

• MyVariant Identifiers: chr1:g.983182G>A (hg19) ; chr1:g.1047802G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1047802G>A , CM000663.2:g.1047802G>A	GRCh38
NC_000001.10:g.983182G>A , CM000663.1:g.983182G>A	GRCh37
NC_000001.9:g.973045G>A	NCBI36
NG_016346.1:g.32680G>A , LRG_198:g.32680G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.3658G>A MANE Select	ENSP00000368678.2:p.Ala1220Thr
ENST00000651234.1:c.3343G>A	ENSP00000499046.1:p.Ala1115Thr
ENST00000652369.1:c.3343G>A	ENSP00000498543.1:p.Ala1115Thr
ENST00000379370.6:c.3658G>A	ENSP00000368678.2:p.Ala1220Thr
ENST00000466223.1:n.396G>A
ENST00000478677.1:n.240G>A
ENST00000620552.4:c.3244G>A	ENSP00000484607.1:p.Ala1082Thr
NM_001305275.1:c.3658G>A	NP_001292204.1:p.Ala1220Thr
NM_198576.3:c.3658G>A	NP_940978.2:p.Ala1220Thr
XM_005244749.2:c.3658G>A	XP_005244806.1:p.Ala1220Thr
XM_006710635.2:c.3658G>A	XP_006710698.1:p.Ala1220Thr
XM_011541429.1:c.3658G>A	XP_011539731.1:p.Ala1220Thr
XM_011541430.1:c.2785G>A	XP_011539732.1:p.Ala929Thr
XM_011541431.1:c.1924G>A	XP_011539733.1:p.Ala642Thr
XR_946650.1:n.3725G>A
NM_001364727.1:c.3343G>A	NP_001351656.1:p.Ala1115Thr
XM_005244749.3:c.3658G>A	XP_005244806.1:p.Ala1220Thr
XM_011541429.2:c.3658G>A	XP_011539731.1:p.Ala1220Thr
XR_946650.2:n.3729G>A
NM_001305275.2:c.3658G>A	NP_001292204.1:p.Ala1220Thr
NM_198576.4:c.3658G>A MANE Select	NP_940978.2:p.Ala1220Thr
NM_001364727.2:c.3343G>A	NP_001351656.1:p.Ala1115Thr