Canonical Allele Identifier: CA337779639

Gene: AGRN

Linked Data

• MyVariant Identifiers: chr1:g.985630T>A (hg19) ; chr1:g.1050250T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1050250T>A , CM000663.2:g.1050250T>A	GRCh38
NC_000001.10:g.985630T>A , CM000663.1:g.985630T>A	GRCh37
NC_000001.9:g.975493T>A	NCBI36
NG_016346.1:g.35128T>A , LRG_198:g.35128T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.4897T>A MANE Select	ENSP00000368678.2:p.Ser1633Thr
ENST00000651234.1:c.4582T>A	ENSP00000499046.1:p.Ser1528Thr
ENST00000652369.1:c.4582T>A	ENSP00000498543.1:p.Ser1528Thr
ENST00000379370.6:c.4897T>A	ENSP00000368678.2:p.Ser1633Thr
ENST00000620552.4:c.4483T>A	ENSP00000484607.1:p.Ser1495Thr
NM_001305275.1:c.4897T>A	NP_001292204.1:p.Ser1633Thr
NM_198576.3:c.4897T>A	NP_940978.2:p.Ser1633Thr
XM_005244749.2:c.4897T>A	XP_005244806.1:p.Ser1633Thr
XM_006710635.2:c.4897T>A	XP_006710698.1:p.Ser1633Thr
XM_011541429.1:c.4897T>A	XP_011539731.1:p.Ser1633Thr
XM_011541430.1:c.4024T>A	XP_011539732.1:p.Ser1342Thr
XM_011541431.1:c.3163T>A	XP_011539733.1:p.Ser1055Thr
XR_946650.1:n.4964T>A
NM_001364727.1:c.4582T>A	NP_001351656.1:p.Ser1528Thr
XM_005244749.3:c.4897T>A	XP_005244806.1:p.Ser1633Thr
XM_011541429.2:c.4897T>A	XP_011539731.1:p.Ser1633Thr
XR_946650.2:n.4968T>A
NM_001305275.2:c.4897T>A	NP_001292204.1:p.Ser1633Thr
NM_198576.4:c.4897T>A MANE Select	NP_940978.2:p.Ser1633Thr
NM_001364727.2:c.4582T>A	NP_001351656.1:p.Ser1528Thr