Canonical Allele Identifier: CA516139296

Linked Data

MyVariant Identifiers: chrX:g.43809034A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43949788A>C , CM000685.2:g.43949788A>C GRCh38
NC_000023.10:g.43809034A>C , CM000685.1:g.43809034A>C GRCh37
NC_000023.9:g.43693978A>C NCBI36
NG_009832.1:g.28888T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000642620.1:c.*11T>G (NDP) MANE Select ENSP00000495972.1:n.*11T>G
ENST00000647044.1:c.*11T>G (NDP) ENSP00000495811.1:n.*11T>G
ENST00000378062.5:c.*11T>G (NDP) ENSP00000367301.5:n.*11T>G
ENST00000470584.1:n.457T>G (NDP)
NM_000266.3:c.*11T>G (NDP) NP_000257.1:n.*11T>G
NR_046631.1:n.57A>C (NDP-AS1)
NM_000266.4:c.*11T>G (NDP) MANE Select NP_000257.1:n.*11T>G