Canonical Allele Identifier: CA2164294901
Gene: MAGEL2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.23644463C= , CM000677.2:g.23644463C= GRCh38
NC_000015.9:g.23889610C= , CM000677.1:g.23889610C= GRCh37
NC_000015.8:g.21440703C= NCBI36
NG_016776.1:g.8384G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650528.1:c.3280G= MANE Select ENSP00000497810.1:p.Gly1094=
ENST00000532292.2:c.3280G= ENSP00000433433.2:p.Gly1094=
NM_019066.4:c.3280G= NP_061939.3:p.Gly1094=
NM_019066.5:c.3280G= MANE Select NP_061939.3:p.Gly1094=
Search 100 bp 5'
Search 100 bp 3'