Canonical Allele Identifier: CA872279117

Gene: MAGEC3

Linked Data

• dbSNP Id: rs1556437463
• MyVariant Identifiers: chrX:g.140982885_140982886insGGGGGGGAAC (hg19) ; chrX:g.141895099_141895100insGGGGGGGAAC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.141895102_141895103insGGGGAACGGG , CM000685.2:g.141895102_141895103insGGGGAACGGG	GRCh38
NC_000023.10:g.140982888_140982889insGGGGAACGGG , CM000685.1:g.140982888_140982889insGGGGAACGGG	GRCh37
NC_000023.9:g.140810554_140810555insGGGGAACGGG	NCBI36
NG_013272.1:g.61787_61788insGGGGAACGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298296.1:c.910-167_910-166insGGGGAACGGG MANE Select	ENSP00000298296.1:n.910-167_910-166insGGGGAACGGG
ENST00000443323.2:c.-118-1329_-118-1328insGGGGAACGGG	ENSP00000438254.1:n.-118-1329_-118-1328insGGGGAACGGG
ENST00000483584.5:n.150-167_150-166insGGGGAACGGG
ENST00000544766.5:c.-378-167_-378-166insGGGGAACGGG	ENSP00000440444.1:n.-378-167_-378-166insGGGGAACGGG
NM_138702.1:c.910-167_910-166insGGGGAACGGG MANE Select	NP_619647.1:n.910-167_910-166insGGGGAACGGG
NM_177456.2:c.-378-167_-378-166insGGGGAACGGG	NP_803251.1:n.-378-167_-378-166insGGGGAACGGG
XM_017029265.2:c.-378-167_-378-166insGGGGAACGGG	XP_016884754.1:n.-378-167_-378-166insGGGGAACGGG