Canonical Allele Identifier: CA516139438

Linked Data

MyVariant Identifiers: chrX:g.43809120T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43949874T>A , CM000685.2:g.43949874T>A GRCh38
NC_000023.10:g.43809120T>A , CM000685.1:g.43809120T>A GRCh37
NC_000023.9:g.43694064T>A NCBI36
NG_009832.1:g.28802A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000642620.1:c.327A>T (NDP) MANE Select ENSP00000495972.1:p.Arg109=
ENST00000647044.1:c.327A>T (NDP) ENSP00000495811.1:p.Arg109=
ENST00000378062.5:c.327A>T (NDP) ENSP00000367301.5:p.Arg109=
ENST00000470584.1:n.371A>T (NDP)
NM_000266.3:c.327A>T (NDP) NP_000257.1:p.Arg109=
NR_046631.1:n.143T>A (NDP-AS1)
NM_000266.4:c.327A>T (NDP) MANE Select NP_000257.1:p.Arg109=