Canonical Allele Identifier: CA412974032
Gene: XK HGNC NCBI

Linked Data

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

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

Transcript Alleles

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