Canonical Allele Identifier: CA337779332

Gene: AGRN

Linked Data

• MyVariant Identifiers: chr1:g.985294G>A (hg19) ; chr1:g.1049914G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1049914G>A , CM000663.2:g.1049914G>A	GRCh38
NC_000001.10:g.985294G>A , CM000663.1:g.985294G>A	GRCh37
NC_000001.9:g.975157G>A	NCBI36
NG_016346.1:g.34792G>A , LRG_198:g.34792G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.4756G>A MANE Select	ENSP00000368678.2:p.Ala1586Thr
ENST00000651234.1:c.4441G>A	ENSP00000499046.1:p.Ala1481Thr
ENST00000652369.1:c.4441G>A	ENSP00000498543.1:p.Ala1481Thr
ENST00000379370.6:c.4756G>A	ENSP00000368678.2:p.Ala1586Thr
ENST00000620552.4:c.4342G>A	ENSP00000484607.1:p.Ala1448Thr
NM_001305275.1:c.4756G>A	NP_001292204.1:p.Ala1586Thr
NM_198576.3:c.4756G>A	NP_940978.2:p.Ala1586Thr
XM_005244749.2:c.4756G>A	XP_005244806.1:p.Ala1586Thr
XM_006710635.2:c.4756G>A	XP_006710698.1:p.Ala1586Thr
XM_011541429.1:c.4756G>A	XP_011539731.1:p.Ala1586Thr
XM_011541430.1:c.3883G>A	XP_011539732.1:p.Ala1295Thr
XM_011541431.1:c.3022G>A	XP_011539733.1:p.Ala1008Thr
XR_946650.1:n.4823G>A
NM_001364727.1:c.4441G>A	NP_001351656.1:p.Ala1481Thr
XM_005244749.3:c.4756G>A	XP_005244806.1:p.Ala1586Thr
XM_011541429.2:c.4756G>A	XP_011539731.1:p.Ala1586Thr
XR_946650.2:n.4827G>A
NM_001305275.2:c.4756G>A	NP_001292204.1:p.Ala1586Thr
NM_198576.4:c.4756G>A MANE Select	NP_940978.2:p.Ala1586Thr
NM_001364727.2:c.4441G>A	NP_001351656.1:p.Ala1481Thr