Canonical Allele Identifier: CA391323567

Gene: MAGEL2

Linked Data

• MyVariant Identifiers: chr15:g.23889562A>G (hg19) ; chr15:g.23644415A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.23644415A>G , CM000677.2:g.23644415A>G	GRCh38
NC_000015.9:g.23889562A>G , CM000677.1:g.23889562A>G	GRCh37
NC_000015.8:g.21440655A>G	NCBI36
NG_016776.1:g.8432T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650528.1:c.3328T>C MANE Select	ENSP00000497810.1:p.Phe1110Leu
ENST00000532292.2:c.3328T>C	ENSP00000433433.2:p.Phe1110Leu
NM_019066.4:c.3328T>C	NP_061939.3:p.Phe1110Leu
NM_019066.5:c.3328T>C MANE Select	NP_061939.3:p.Phe1110Leu