Canonical Allele Identifier: CA412974034
Gene: XK HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.37587067T>A (hg19) chrX:g.37727814T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37727814T>A , CM000685.2:g.37727814T>A GRCh38
NC_000023.10:g.37587067T>A , CM000685.1:g.37587067T>A GRCh37
NC_000023.9:g.37472006T>A NCBI36
NG_007473.1:g.46955T>A
NG_007473.3:g.46935T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378616.5:c.687T>A MANE Select ENSP00000367879.3:p.Phe229Leu
ENST00000378616.3:c.687T>A ENSP00000367879.3:p.Phe229Leu
ENST00000465127.1:c.171+301814T>A ENSP00000417050.1:n.171+301814T>A
NM_021083.2:c.687T>A NP_066569.1:p.Phe229Leu
NM_021083.4:c.687T>A MANE Select NP_066569.1:p.Phe229Leu
Search 100 bp 5'
Search 100 bp 3'