Canonical Allele Identifier: CA509762

Gene: AGRN

Linked Data

• dbSNP Id: rs773269271
• ExAC: 1:985641 C / T
• gnomAD v2: 1-985641-C-T
• gnomAD v4: 1-1050261-C-T
• MyVariant Identifiers: chr1:g.985641C>T (hg19) ; chr1:g.1050261C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1050261C>T , CM000663.2:g.1050261C>T	GRCh38
NC_000001.10:g.985641C>T , CM000663.1:g.985641C>T	GRCh37
NC_000001.9:g.975504C>T	NCBI36
NG_016346.1:g.35139C>T , LRG_198:g.35139C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.4908C>T MANE Select	ENSP00000368678.2:p.Phe1636=
ENST00000651234.1:c.4593C>T	ENSP00000499046.1:p.Phe1531=
ENST00000652369.1:c.4593C>T	ENSP00000498543.1:p.Phe1531=
ENST00000379370.6:c.4908C>T	ENSP00000368678.2:p.Phe1636=
ENST00000620552.4:c.4494C>T	ENSP00000484607.1:p.Phe1498=
NM_001305275.1:c.4908C>T	NP_001292204.1:p.Phe1636=
NM_198576.3:c.4908C>T	NP_940978.2:p.Phe1636=
XM_005244749.2:c.4908C>T	XP_005244806.1:p.Phe1636=
XM_006710635.2:c.4908C>T	XP_006710698.1:p.Phe1636=
XM_011541429.1:c.4908C>T	XP_011539731.1:p.Phe1636=
XM_011541430.1:c.4035C>T	XP_011539732.1:p.Phe1345=
XM_011541431.1:c.3174C>T	XP_011539733.1:p.Phe1058=
XR_946650.1:n.4975C>T
NM_001364727.1:c.4593C>T	NP_001351656.1:p.Phe1531=
XM_005244749.3:c.4908C>T	XP_005244806.1:p.Phe1636=
XM_011541429.2:c.4908C>T	XP_011539731.1:p.Phe1636=
XR_946650.2:n.4979C>T
NM_001305275.2:c.4908C>T	NP_001292204.1:p.Phe1636=
NM_198576.4:c.4908C>T MANE Select	NP_940978.2:p.Phe1636=
NM_001364727.2:c.4593C>T	NP_001351656.1:p.Phe1531=