Canonical Allele Identifier: CA10532736

Gene: MAGEC3

Linked Data

• dbSNP Id: rs367831409
• ExAC: X:140983242 A / C
• gnomAD v2: X-140983242-A-C
• gnomAD v3: X-141895456-A-C
• gnomAD v4: X-141895456-A-C
• MyVariant Identifiers: chrX:g.140983242A>C (hg19) ; chrX:g.141895456A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.141895456A>C , CM000685.2:g.141895456A>C	GRCh38
NC_000023.10:g.140983242A>C , CM000685.1:g.140983242A>C	GRCh37
NC_000023.9:g.140810908A>C	NCBI36
NG_013272.1:g.62141A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298296.1:c.1049-29A>C MANE Select	ENSP00000298296.1:n.1049-29A>C
ENST00000443323.2:c.-118-975A>C	ENSP00000438254.1:n.-118-975A>C
ENST00000483584.5:n.288+49A>C
ENST00000544766.5:c.-240+49A>C	ENSP00000440444.1:n.-240+49A>C
NM_138702.1:c.1049-29A>C MANE Select	NP_619647.1:n.1049-29A>C
NM_177456.2:c.-240+49A>C	NP_803251.1:n.-240+49A>C
XM_011531267.1:c.-163+49A>C	XP_011529569.1:n.-163+49A>C
XM_011531267.3:c.-163+49A>C	XP_011529569.1:n.-163+49A>C
XM_017029265.2:c.-240+49A>C	XP_016884754.1:n.-240+49A>C