Canonical Allele Identifier: CA2694863428

Gene: MAGEC3

Linked Data

• gnomAD v4: X-141895708-C-CCTG

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.141895708_141895709insCTG , CM000685.2:g.141895708_141895709insCTG	GRCh38
NC_000023.10:g.140983494_140983495insCTG , CM000685.1:g.140983494_140983495insCTG	GRCh37
NC_000023.9:g.140811160_140811161insCTG	NCBI36
NG_013272.1:g.62393_62394insCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298296.1:c.1123+149_1123+150insCTG MANE Select	ENSP00000298296.1:n.1123+149_1123+150insCTG
ENST00000443323.2:c.-118-723_-118-722insCTG	ENSP00000438254.1:n.-118-723_-118-722insCTG
ENST00000483584.5:n.288+301_288+302insCTG
ENST00000544766.5:c.-240+301_-240+302insCTG	ENSP00000440444.1:n.-240+301_-240+302insCTG
NM_138702.1:c.1123+149_1123+150insCTG MANE Select	NP_619647.1:n.1123+149_1123+150insCTG
NM_177456.2:c.-240+301_-240+302insCTG	NP_803251.1:n.-240+301_-240+302insCTG
XM_011531267.1:c.-163+301_-163+302insCTG	XP_011529569.1:n.-163+301_-163+302insCTG
XM_011531267.3:c.-163+301_-163+302insCTG	XP_011529569.1:n.-163+301_-163+302insCTG
XM_017029265.2:c.-240+301_-240+302insCTG	XP_016884754.1:n.-240+301_-240+302insCTG