Canonical Allele Identifier: CA415758835

Gene: AGRN

Linked Data

• MyVariant Identifiers: chr1:g.985653C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1050273C>T , CM000663.2:g.1050273C>T	GRCh38
NC_000001.10:g.985653C>T , CM000663.1:g.985653C>T	GRCh37
NC_000001.9:g.975516C>T	NCBI36
NG_016346.1:g.35151C>T , LRG_198:g.35151C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.4920C>T MANE Select	ENSP00000368678.2:p.Phe1640=
ENST00000651234.1:c.4605C>T	ENSP00000499046.1:p.Phe1535=
ENST00000652369.1:c.4605C>T	ENSP00000498543.1:p.Phe1535=
ENST00000379370.6:c.4920C>T	ENSP00000368678.2:p.Phe1640=
ENST00000620552.4:c.4506C>T	ENSP00000484607.1:p.Phe1502=
NM_001305275.1:c.4920C>T	NP_001292204.1:p.Phe1640=
NM_198576.3:c.4920C>T	NP_940978.2:p.Phe1640=
XM_005244749.2:c.4920C>T	XP_005244806.1:p.Phe1640=
XM_006710635.2:c.4920C>T	XP_006710698.1:p.Phe1640=
XM_011541429.1:c.4920C>T	XP_011539731.1:p.Phe1640=
XM_011541430.1:c.4047C>T	XP_011539732.1:p.Phe1349=
XM_011541431.1:c.3186C>T	XP_011539733.1:p.Phe1062=
XR_946650.1:n.4987C>T
NM_001364727.1:c.4605C>T	NP_001351656.1:p.Phe1535=
XM_005244749.3:c.4920C>T	XP_005244806.1:p.Phe1640=
XM_011541429.2:c.4920C>T	XP_011539731.1:p.Phe1640=
XR_946650.2:n.4991C>T
NM_001305275.2:c.4920C>T	NP_001292204.1:p.Phe1640=
NM_198576.4:c.4920C>T MANE Select	NP_940978.2:p.Phe1640=
NM_001364727.2:c.4605C>T	NP_001351656.1:p.Phe1535=