Canonical Allele Identifier: CA1148803867

Gene: AGRN

Linked Data

• dbSNP Id: rs1644419124

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1022132C>A , CM000663.2:g.1022132C>A	GRCh38
NC_000001.10:g.957512C>A , CM000663.1:g.957512C>A	GRCh37
NC_000001.9:g.947375C>A	NCBI36
NG_016346.1:g.7010C>A , LRG_198:g.7010C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.202-69C>A MANE Select	ENSP00000368678.2:n.202-69C>A
ENST00000379370.6:c.202-69C>A	ENSP00000368678.2:n.202-69C>A
ENST00000620552.4:c.-213-69C>A	ENSP00000484607.1:n.-213-69C>A
NM_001305275.1:c.202-69C>A	NP_001292204.1:n.202-69C>A
NM_198576.3:c.202-69C>A	NP_940978.2:n.202-69C>A
XM_005244749.2:c.202-69C>A	XP_005244806.1:n.202-69C>A
XM_006710635.2:c.202-69C>A	XP_006710698.1:n.202-69C>A
XM_011541429.1:c.202-69C>A	XP_011539731.1:n.202-69C>A
XM_011541430.1:c.202-69C>A	XP_011539732.1:n.202-69C>A
XR_946650.1:n.269-69C>A
XM_005244749.3:c.202-69C>A	XP_005244806.1:n.202-69C>A
XM_011541429.2:c.202-69C>A	XP_011539731.1:n.202-69C>A
XR_946650.2:n.273-69C>A
NM_001305275.2:c.202-69C>A	NP_001292204.1:n.202-69C>A
NM_198576.4:c.202-69C>A MANE Select	NP_940978.2:n.202-69C>A