Canonical Allele Identifier: CA1137911131

Gene: MAGEC3

Linked Data

• gnomAD v3: X-141895103-T-TGGGAACGGGG
• gnomAD v4: X-141895103-T-TGGGAACGGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.141895107_141895108insACGGGGGGGA , CM000685.2:g.141895107_141895108insACGGGGGGGA	GRCh38
NC_000023.10:g.140982893_140982894insACGGGGGGGA , CM000685.1:g.140982893_140982894insACGGGGGGGA	GRCh37
NC_000023.9:g.140810559_140810560insACGGGGGGGA	NCBI36
NG_013272.1:g.61792_61793insACGGGGGGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298296.1:c.910-162_910-161insACGGGGGGGA MANE Select	ENSP00000298296.1:n.910-162_910-161insACGGGGGGGA
ENST00000443323.2:c.-118-1324_-118-1323insACGGGGGGGA	ENSP00000438254.1:n.-118-1324_-118-1323insACGGGGGGGA
ENST00000483584.5:n.150-162_150-161insACGGGGGGGA
ENST00000544766.5:c.-378-162_-378-161insACGGGGGGGA	ENSP00000440444.1:n.-378-162_-378-161insACGGGGGGGA
NM_138702.1:c.910-162_910-161insACGGGGGGGA MANE Select	NP_619647.1:n.910-162_910-161insACGGGGGGGA
NM_177456.2:c.-378-162_-378-161insACGGGGGGGA	NP_803251.1:n.-378-162_-378-161insACGGGGGGGA
XM_017029265.2:c.-378-162_-378-161insACGGGGGGGA	XP_016884754.1:n.-378-162_-378-161insACGGGGGGGA