Canonical Allele Identifier: CA645125949

Gene: MAGEC3

Linked Data

• dbSNP Id: rs1348765653
• gnomAD v2: X-140983377-C-T
• COSMIC: COSN18042986
• MyVariant Identifiers: chrX:g.140983377C>T (hg19) ; chrX:g.141895591C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.141895591C>T , CM000685.2:g.141895591C>T	GRCh38
NC_000023.10:g.140983377C>T , CM000685.1:g.140983377C>T	GRCh37
NC_000023.9:g.140811043C>T	NCBI36
NG_013272.1:g.62276C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298296.1:c.1123+32C>T MANE Select	ENSP00000298296.1:n.1123+32C>T
ENST00000443323.2:c.-118-840C>T	ENSP00000438254.1:n.-118-840C>T
ENST00000483584.5:n.288+184C>T
ENST00000544766.5:c.-240+184C>T	ENSP00000440444.1:n.-240+184C>T
NM_138702.1:c.1123+32C>T MANE Select	NP_619647.1:n.1123+32C>T
NM_177456.2:c.-240+184C>T	NP_803251.1:n.-240+184C>T
XM_011531267.1:c.-163+184C>T	XP_011529569.1:n.-163+184C>T
XM_011531267.3:c.-163+184C>T	XP_011529569.1:n.-163+184C>T
XM_017029265.2:c.-240+184C>T	XP_016884754.1:n.-240+184C>T