Canonical Allele Identifier: CA337834336

Gene: AGRN

Linked Data

• MyVariant Identifiers: chr1:g.979212G>T (hg19) ; chr1:g.1043832G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1043832G>T , CM000663.2:g.1043832G>T	GRCh38
NC_000001.10:g.979212G>T , CM000663.1:g.979212G>T	GRCh37
NC_000001.9:g.969075G>T	NCBI36
NG_016346.1:g.28710G>T , LRG_198:g.28710G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.1808G>T MANE Select	ENSP00000368678.2:p.Gly603Val
ENST00000651234.1:c.1493G>T	ENSP00000499046.1:p.Gly498Val
ENST00000652369.1:c.1493G>T	ENSP00000498543.1:p.Gly498Val
ENST00000379370.6:c.1808G>T	ENSP00000368678.2:p.Gly603Val
ENST00000620552.4:c.1394G>T	ENSP00000484607.1:p.Gly465Val
NM_001305275.1:c.1808G>T	NP_001292204.1:p.Gly603Val
NM_198576.3:c.1808G>T	NP_940978.2:p.Gly603Val
XM_005244749.2:c.1808G>T	XP_005244806.1:p.Gly603Val
XM_006710635.2:c.1808G>T	XP_006710698.1:p.Gly603Val
XM_011541429.1:c.1808G>T	XP_011539731.1:p.Gly603Val
XM_011541430.1:c.935G>T	XP_011539732.1:p.Gly312Val
XM_011541431.1:c.74G>T	XP_011539733.1:p.Gly25Val
XR_946650.1:n.1875G>T
NM_001364727.1:c.1493G>T	NP_001351656.1:p.Gly498Val
XM_005244749.3:c.1808G>T	XP_005244806.1:p.Gly603Val
XM_011541429.2:c.1808G>T	XP_011539731.1:p.Gly603Val
XR_946650.2:n.1879G>T
NM_001305275.2:c.1808G>T	NP_001292204.1:p.Gly603Val
NM_198576.4:c.1808G>T MANE Select	NP_940978.2:p.Gly603Val
NM_001364727.2:c.1493G>T	NP_001351656.1:p.Gly498Val