Canonical Allele Identifier: CA2462229918
Gene: MAGEC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.141895676_141895679delinsGCTC , CM000685.2:g.141895676_141895679delinsGCTC GRCh38
NC_000023.10:g.140983462_140983465delinsGCTC , CM000685.1:g.140983462_140983465delinsGCTC GRCh37
NC_000023.9:g.140811128_140811131delinsGCTC NCBI36
NG_013272.1:g.62361_62364delinsGCTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000298296.1:c.1123+117_1123+120delinsGCTC MANE Select ENSP00000298296.1:n.1123+117_1123+120delinsGCTC
ENST00000443323.2:c.-118-755_-118-752delinsGCTC ENSP00000438254.1:n.-118-755_-118-752delinsGCTC
ENST00000483584.5:n.288+269_288+272delinsGCTC
ENST00000544766.5:c.-240+269_-240+272delinsGCTC ENSP00000440444.1:n.-240+269_-240+272delinsGCTC
NM_138702.1:c.1123+117_1123+120delinsGCTC MANE Select NP_619647.1:n.1123+117_1123+120delinsGCTC
NM_177456.2:c.-240+269_-240+272delinsGCTC NP_803251.1:n.-240+269_-240+272delinsGCTC
XM_011531267.1:c.-163+269_-163+272delinsGCTC XP_011529569.1:n.-163+269_-163+272delinsGCTC
XM_011531267.3:c.-163+269_-163+272delinsGCTC XP_011529569.1:n.-163+269_-163+272delinsGCTC
XM_017029265.2:c.-240+269_-240+272delinsGCTC XP_016884754.1:n.-240+269_-240+272delinsGCTC