Canonical Allele Identifier: CA412974406
Gene: XK HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.37587152T>A (hg19) chrX:g.37727899T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37727899T>A , CM000685.2:g.37727899T>A GRCh38
NC_000023.10:g.37587152T>A , CM000685.1:g.37587152T>A GRCh37
NC_000023.9:g.37472091T>A NCBI36
NG_007473.1:g.47040T>A
NG_007473.3:g.47020T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378616.5:c.772T>A MANE Select ENSP00000367879.3:p.Cys258Ser
ENST00000378616.3:c.772T>A ENSP00000367879.3:p.Cys258Ser
ENST00000465127.1:c.171+301899T>A ENSP00000417050.1:n.171+301899T>A
NM_021083.2:c.772T>A NP_066569.1:p.Cys258Ser
NM_021083.4:c.772T>A MANE Select NP_066569.1:p.Cys258Ser
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