Canonical Allele Identifier: CA415756985

Gene: AGRN

Linked Data

• MyVariant Identifiers: chr1:g.979363G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1043983G>A , CM000663.2:g.1043983G>A	GRCh38
NC_000001.10:g.979363G>A , CM000663.1:g.979363G>A	GRCh37
NC_000001.9:g.969226G>A	NCBI36
NG_016346.1:g.28861G>A , LRG_198:g.28861G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.1959G>A MANE Select	ENSP00000368678.2:p.Gln653=
ENST00000651234.1:c.1644G>A	ENSP00000499046.1:p.Gln548=
ENST00000652369.1:c.1644G>A	ENSP00000498543.1:p.Gln548=
ENST00000379370.6:c.1959G>A	ENSP00000368678.2:p.Gln653=
ENST00000620552.4:c.1545G>A	ENSP00000484607.1:p.Gln515=
NM_001305275.1:c.1959G>A	NP_001292204.1:p.Gln653=
NM_198576.3:c.1959G>A	NP_940978.2:p.Gln653=
XM_005244749.2:c.1959G>A	XP_005244806.1:p.Gln653=
XM_006710635.2:c.1959G>A	XP_006710698.1:p.Gln653=
XM_011541429.1:c.1959G>A	XP_011539731.1:p.Gln653=
XM_011541430.1:c.1086G>A	XP_011539732.1:p.Gln362=
XM_011541431.1:c.225G>A	XP_011539733.1:p.Gln75=
XR_946650.1:n.2026G>A
NM_001364727.1:c.1644G>A	NP_001351656.1:p.Gln548=
XM_005244749.3:c.1959G>A	XP_005244806.1:p.Gln653=
XM_011541429.2:c.1959G>A	XP_011539731.1:p.Gln653=
XR_946650.2:n.2030G>A
NM_001305275.2:c.1959G>A	NP_001292204.1:p.Gln653=
NM_198576.4:c.1959G>A MANE Select	NP_940978.2:p.Gln653=
NM_001364727.2:c.1644G>A	NP_001351656.1:p.Gln548=