Canonical Allele Identifier: CA337779323

Gene: AGRN

Linked Data

• gnomAD v4: 1-1049909-C-A
• MyVariant Identifiers: chr1:g.985289C>A (hg19) ; chr1:g.1049909C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1049909C>A , CM000663.2:g.1049909C>A	GRCh38
NC_000001.10:g.985289C>A , CM000663.1:g.985289C>A	GRCh37
NC_000001.9:g.975152C>A	NCBI36
NG_016346.1:g.34787C>A , LRG_198:g.34787C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.4751C>A MANE Select	ENSP00000368678.2:p.Thr1584Asn
ENST00000651234.1:c.4436C>A	ENSP00000499046.1:p.Thr1479Asn
ENST00000652369.1:c.4436C>A	ENSP00000498543.1:p.Thr1479Asn
ENST00000379370.6:c.4751C>A	ENSP00000368678.2:p.Thr1584Asn
ENST00000620552.4:c.4337C>A	ENSP00000484607.1:p.Thr1446Asn
NM_001305275.1:c.4751C>A	NP_001292204.1:p.Thr1584Asn
NM_198576.3:c.4751C>A	NP_940978.2:p.Thr1584Asn
XM_005244749.2:c.4751C>A	XP_005244806.1:p.Thr1584Asn
XM_006710635.2:c.4751C>A	XP_006710698.1:p.Thr1584Asn
XM_011541429.1:c.4751C>A	XP_011539731.1:p.Thr1584Asn
XM_011541430.1:c.3878C>A	XP_011539732.1:p.Thr1293Asn
XM_011541431.1:c.3017C>A	XP_011539733.1:p.Thr1006Asn
XR_946650.1:n.4818C>A
NM_001364727.1:c.4436C>A	NP_001351656.1:p.Thr1479Asn
XM_005244749.3:c.4751C>A	XP_005244806.1:p.Thr1584Asn
XM_011541429.2:c.4751C>A	XP_011539731.1:p.Thr1584Asn
XR_946650.2:n.4822C>A
NM_001305275.2:c.4751C>A	NP_001292204.1:p.Thr1584Asn
NM_198576.4:c.4751C>A MANE Select	NP_940978.2:p.Thr1584Asn
NM_001364727.2:c.4436C>A	NP_001351656.1:p.Thr1479Asn