Canonical Allele Identifier: CA337835804

Gene: AGRN

Linked Data

• ClinVar Variation Id: 1076092
• ClinVar RCV Id: RCV001389873
• dbSNP Id: rs199801106
• MyVariant Identifiers: chr1:g.979491G>T (hg19) ; chr1:g.1044111G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1044111G>T , CM000663.2:g.1044111G>T	GRCh38
NC_000001.10:g.979491G>T , CM000663.1:g.979491G>T	GRCh37
NC_000001.9:g.969354G>T	NCBI36
NG_016346.1:g.28989G>T , LRG_198:g.28989G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.2002G>T MANE Select	ENSP00000368678.2:p.Glu668Ter
ENST00000651234.1:c.1687G>T	ENSP00000499046.1:p.Glu563Ter
ENST00000652369.1:c.1687G>T	ENSP00000498543.1:p.Glu563Ter
ENST00000379370.6:c.2002G>T	ENSP00000368678.2:p.Glu668Ter
ENST00000620552.4:c.1588G>T	ENSP00000484607.1:p.Glu530Ter
NM_001305275.1:c.2002G>T	NP_001292204.1:p.Glu668Ter
NM_198576.3:c.2002G>T	NP_940978.2:p.Glu668Ter
XM_005244749.2:c.2002G>T	XP_005244806.1:p.Glu668Ter
XM_006710635.2:c.2002G>T	XP_006710698.1:p.Glu668Ter
XM_011541429.1:c.2002G>T	XP_011539731.1:p.Glu668Ter
XM_011541430.1:c.1129G>T	XP_011539732.1:p.Glu377Ter
XM_011541431.1:c.268G>T	XP_011539733.1:p.Glu90Ter
XR_946650.1:n.2069G>T
NM_001364727.1:c.1687G>T	NP_001351656.1:p.Glu563Ter
XM_005244749.3:c.2002G>T	XP_005244806.1:p.Glu668Ter
XM_011541429.2:c.2002G>T	XP_011539731.1:p.Glu668Ter
XR_946650.2:n.2073G>T
NM_001305275.2:c.2002G>T	NP_001292204.1:p.Glu668Ter
NM_198576.4:c.2002G>T MANE Select	NP_940978.2:p.Glu668Ter
NM_001364727.2:c.1687G>T	NP_001351656.1:p.Glu563Ter