Canonical Allele Identifier: CA515942727
Gene: XK HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.37587070C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37727817C>G , CM000685.2:g.37727817C>G GRCh38
NC_000023.10:g.37587070C>G , CM000685.1:g.37587070C>G GRCh37
NC_000023.9:g.37472009C>G NCBI36
NG_007473.1:g.46958C>G
NG_007473.3:g.46938C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378616.5:c.690C>G MANE Select ENSP00000367879.3:p.Thr230=
ENST00000378616.3:c.690C>G ENSP00000367879.3:p.Thr230=
ENST00000465127.1:c.171+301817C>G ENSP00000417050.1:n.171+301817C>G
NM_021083.2:c.690C>G NP_066569.1:p.Thr230=
NM_021083.4:c.690C>G MANE Select NP_066569.1:p.Thr230=