Canonical Allele Identifier: CA337779376

Gene: AGRN

Linked Data

• gnomAD v4: 1-1049932-T-G
• MyVariant Identifiers: chr1:g.985312T>G (hg19) ; chr1:g.1049932T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1049932T>G , CM000663.2:g.1049932T>G	GRCh38
NC_000001.10:g.985312T>G , CM000663.1:g.985312T>G	GRCh37
NC_000001.9:g.975175T>G	NCBI36
NG_016346.1:g.34810T>G , LRG_198:g.34810T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.4774T>G MANE Select	ENSP00000368678.2:p.Cys1592Gly
ENST00000651234.1:c.4459T>G	ENSP00000499046.1:p.Cys1487Gly
ENST00000652369.1:c.4459T>G	ENSP00000498543.1:p.Cys1487Gly
ENST00000379370.6:c.4774T>G	ENSP00000368678.2:p.Cys1592Gly
ENST00000620552.4:c.4360T>G	ENSP00000484607.1:p.Cys1454Gly
NM_001305275.1:c.4774T>G	NP_001292204.1:p.Cys1592Gly
NM_198576.3:c.4774T>G	NP_940978.2:p.Cys1592Gly
XM_005244749.2:c.4774T>G	XP_005244806.1:p.Cys1592Gly
XM_006710635.2:c.4774T>G	XP_006710698.1:p.Cys1592Gly
XM_011541429.1:c.4774T>G	XP_011539731.1:p.Cys1592Gly
XM_011541430.1:c.3901T>G	XP_011539732.1:p.Cys1301Gly
XM_011541431.1:c.3040T>G	XP_011539733.1:p.Cys1014Gly
XR_946650.1:n.4841T>G
NM_001364727.1:c.4459T>G	NP_001351656.1:p.Cys1487Gly
XM_005244749.3:c.4774T>G	XP_005244806.1:p.Cys1592Gly
XM_011541429.2:c.4774T>G	XP_011539731.1:p.Cys1592Gly
XR_946650.2:n.4845T>G
NM_001305275.2:c.4774T>G	NP_001292204.1:p.Cys1592Gly
NM_198576.4:c.4774T>G MANE Select	NP_940978.2:p.Cys1592Gly
NM_001364727.2:c.4459T>G	NP_001351656.1:p.Cys1487Gly