Canonical Allele Identifier: CA337851164

Gene: AGRN

Linked Data

• MyVariant Identifiers: chr1:g.983161G>T (hg19) ; chr1:g.1047781G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1047781G>T , CM000663.2:g.1047781G>T	GRCh38
NC_000001.10:g.983161G>T , CM000663.1:g.983161G>T	GRCh37
NC_000001.9:g.973024G>T	NCBI36
NG_016346.1:g.32659G>T , LRG_198:g.32659G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.3637G>T MANE Select	ENSP00000368678.2:p.Ala1213Ser
ENST00000651234.1:c.3322G>T	ENSP00000499046.1:p.Ala1108Ser
ENST00000652369.1:c.3322G>T	ENSP00000498543.1:p.Ala1108Ser
ENST00000379370.6:c.3637G>T	ENSP00000368678.2:p.Ala1213Ser
ENST00000466223.1:n.375G>T
ENST00000478677.1:n.219G>T
ENST00000620552.4:c.3223G>T	ENSP00000484607.1:p.Ala1075Ser
NM_001305275.1:c.3637G>T	NP_001292204.1:p.Ala1213Ser
NM_198576.3:c.3637G>T	NP_940978.2:p.Ala1213Ser
XM_005244749.2:c.3637G>T	XP_005244806.1:p.Ala1213Ser
XM_006710635.2:c.3637G>T	XP_006710698.1:p.Ala1213Ser
XM_011541429.1:c.3637G>T	XP_011539731.1:p.Ala1213Ser
XM_011541430.1:c.2764G>T	XP_011539732.1:p.Ala922Ser
XM_011541431.1:c.1903G>T	XP_011539733.1:p.Ala635Ser
XR_946650.1:n.3704G>T
NM_001364727.1:c.3322G>T	NP_001351656.1:p.Ala1108Ser
XM_005244749.3:c.3637G>T	XP_005244806.1:p.Ala1213Ser
XM_011541429.2:c.3637G>T	XP_011539731.1:p.Ala1213Ser
XR_946650.2:n.3708G>T
NM_001305275.2:c.3637G>T	NP_001292204.1:p.Ala1213Ser
NM_198576.4:c.3637G>T MANE Select	NP_940978.2:p.Ala1213Ser
NM_001364727.2:c.3322G>T	NP_001351656.1:p.Ala1108Ser