Canonical Allele Identifier: CA516139293

Linked Data

gnomAD v4: X-43949787-C-A
MyVariant Identifiers: chrX:g.43809033C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43949787C>A , CM000685.2:g.43949787C>A GRCh38
NC_000023.10:g.43809033C>A , CM000685.1:g.43809033C>A GRCh37
NC_000023.9:g.43693977C>A NCBI36
NG_009832.1:g.28889G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000642620.1:c.*12G>T (NDP) MANE Select ENSP00000495972.1:n.*12G>T
ENST00000647044.1:c.*12G>T (NDP) ENSP00000495811.1:n.*12G>T
ENST00000378062.5:c.*12G>T (NDP) ENSP00000367301.5:n.*12G>T
ENST00000470584.1:n.458G>T (NDP)
NM_000266.3:c.*12G>T (NDP) NP_000257.1:n.*12G>T
NR_046631.1:n.56C>A (NDP-AS1)
NM_000266.4:c.*12G>T (NDP) MANE Select NP_000257.1:n.*12G>T