Canonical Allele Identifier: CA337812163
Gene: AGRN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1022225G>T , CM000663.2:g.1022225G>T GRCh38
NC_000001.10:g.957605G>T , CM000663.1:g.957605G>T GRCh37
NC_000001.9:g.947468G>T NCBI36
NG_016346.1:g.7103G>T , LRG_198:g.7103G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000379370.7:c.226G>T MANE Select ENSP00000368678.2:p.Gly76Cys
ENST00000379370.6:c.226G>T ENSP00000368678.2:p.Gly76Cys
ENST00000620552.4:c.-189G>T ENSP00000484607.1:n.-189G>T
NM_001305275.1:c.226G>T NP_001292204.1:p.Gly76Cys
NM_198576.3:c.226G>T NP_940978.2:p.Gly76Cys
XM_005244749.2:c.226G>T XP_005244806.1:p.Gly76Cys
XM_006710635.2:c.226G>T XP_006710698.1:p.Gly76Cys
XM_011541429.1:c.226G>T XP_011539731.1:p.Gly76Cys
XM_011541430.1:c.226G>T XP_011539732.1:p.Gly76Cys
XR_946650.1:n.293G>T
XM_005244749.3:c.226G>T XP_005244806.1:p.Gly76Cys
XM_011541429.2:c.226G>T XP_011539731.1:p.Gly76Cys
XR_946650.2:n.297G>T
NM_001305275.2:c.226G>T NP_001292204.1:p.Gly76Cys
NM_198576.4:c.226G>T MANE Select NP_940978.2:p.Gly76Cys