Canonical Allele Identifier: CA2164294877
Gene: MAGEL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.23644414A= , CM000677.2:g.23644414A= GRCh38
NC_000015.9:g.23889561A= , CM000677.1:g.23889561A= GRCh37
NC_000015.8:g.21440654A= NCBI36
NG_016776.1:g.8433T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650528.1:c.3329T= MANE Select ENSP00000497810.1:p.Phe1110=
ENST00000532292.2:c.3329T= ENSP00000433433.2:p.Phe1110=
NM_019066.4:c.3329T= NP_061939.3:p.Phe1110=
NM_019066.5:c.3329T= MANE Select NP_061939.3:p.Phe1110=