Canonical Allele Identifier: CA415757986

Gene: AGRN

Linked Data

• MyVariant Identifiers: chr1:g.983160A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1047780A>G , CM000663.2:g.1047780A>G	GRCh38
NC_000001.10:g.983160A>G , CM000663.1:g.983160A>G	GRCh37
NC_000001.9:g.973023A>G	NCBI36
NG_016346.1:g.32658A>G , LRG_198:g.32658A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.3636A>G MANE Select	ENSP00000368678.2:p.Thr1212=
ENST00000651234.1:c.3321A>G	ENSP00000499046.1:p.Thr1107=
ENST00000652369.1:c.3321A>G	ENSP00000498543.1:p.Thr1107=
ENST00000379370.6:c.3636A>G	ENSP00000368678.2:p.Thr1212=
ENST00000466223.1:n.374A>G
ENST00000478677.1:n.218A>G
ENST00000620552.4:c.3222A>G	ENSP00000484607.1:p.Thr1074=
NM_001305275.1:c.3636A>G	NP_001292204.1:p.Thr1212=
NM_198576.3:c.3636A>G	NP_940978.2:p.Thr1212=
XM_005244749.2:c.3636A>G	XP_005244806.1:p.Thr1212=
XM_006710635.2:c.3636A>G	XP_006710698.1:p.Thr1212=
XM_011541429.1:c.3636A>G	XP_011539731.1:p.Thr1212=
XM_011541430.1:c.2763A>G	XP_011539732.1:p.Thr921=
XM_011541431.1:c.1902A>G	XP_011539733.1:p.Thr634=
XR_946650.1:n.3703A>G
NM_001364727.1:c.3321A>G	NP_001351656.1:p.Thr1107=
XM_005244749.3:c.3636A>G	XP_005244806.1:p.Thr1212=
XM_011541429.2:c.3636A>G	XP_011539731.1:p.Thr1212=
XR_946650.2:n.3707A>G
NM_001305275.2:c.3636A>G	NP_001292204.1:p.Thr1212=
NM_198576.4:c.3636A>G MANE Select	NP_940978.2:p.Thr1212=
NM_001364727.2:c.3321A>G	NP_001351656.1:p.Thr1107=