Canonical Allele Identifier: CA337851200

Gene: AGRN

Linked Data

• MyVariant Identifiers: chr1:g.983165T>G (hg19) ; chr1:g.1047785T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1047785T>G , CM000663.2:g.1047785T>G	GRCh38
NC_000001.10:g.983165T>G , CM000663.1:g.983165T>G	GRCh37
NC_000001.9:g.973028T>G	NCBI36
NG_016346.1:g.32663T>G , LRG_198:g.32663T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.3641T>G MANE Select	ENSP00000368678.2:p.Phe1214Cys
ENST00000651234.1:c.3326T>G	ENSP00000499046.1:p.Phe1109Cys
ENST00000652369.1:c.3326T>G	ENSP00000498543.1:p.Phe1109Cys
ENST00000379370.6:c.3641T>G	ENSP00000368678.2:p.Phe1214Cys
ENST00000466223.1:n.379T>G
ENST00000478677.1:n.223T>G
ENST00000620552.4:c.3227T>G	ENSP00000484607.1:p.Phe1076Cys
NM_001305275.1:c.3641T>G	NP_001292204.1:p.Phe1214Cys
NM_198576.3:c.3641T>G	NP_940978.2:p.Phe1214Cys
XM_005244749.2:c.3641T>G	XP_005244806.1:p.Phe1214Cys
XM_006710635.2:c.3641T>G	XP_006710698.1:p.Phe1214Cys
XM_011541429.1:c.3641T>G	XP_011539731.1:p.Phe1214Cys
XM_011541430.1:c.2768T>G	XP_011539732.1:p.Phe923Cys
XM_011541431.1:c.1907T>G	XP_011539733.1:p.Phe636Cys
XR_946650.1:n.3708T>G
NM_001364727.1:c.3326T>G	NP_001351656.1:p.Phe1109Cys
XM_005244749.3:c.3641T>G	XP_005244806.1:p.Phe1214Cys
XM_011541429.2:c.3641T>G	XP_011539731.1:p.Phe1214Cys
XR_946650.2:n.3712T>G
NM_001305275.2:c.3641T>G	NP_001292204.1:p.Phe1214Cys
NM_198576.4:c.3641T>G MANE Select	NP_940978.2:p.Phe1214Cys
NM_001364727.2:c.3326T>G	NP_001351656.1:p.Phe1109Cys