Canonical Allele Identifier: CA516139246

Linked Data

MyVariant Identifiers: chrX:g.43809021A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43949775A>G , CM000685.2:g.43949775A>G GRCh38
NC_000023.10:g.43809021A>G , CM000685.1:g.43809021A>G GRCh37
NC_000023.9:g.43693965A>G NCBI36
NG_009832.1:g.28901T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000642620.1:c.*24T>C (NDP) MANE Select ENSP00000495972.1:n.*24T>C
ENST00000647044.1:c.*24T>C (NDP) ENSP00000495811.1:n.*24T>C
ENST00000378062.5:c.*24T>C (NDP) ENSP00000367301.5:n.*24T>C
ENST00000470584.1:n.470T>C (NDP)
NM_000266.3:c.*24T>C (NDP) NP_000257.1:n.*24T>C
NR_046631.1:n.44A>G (NDP-AS1)
NM_000266.4:c.*24T>C (NDP) MANE Select NP_000257.1:n.*24T>C