Canonical Allele Identifier: CA2424657842
Gene: XK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37727821G= , CM000685.2:g.37727821G= GRCh38
NC_000023.10:g.37587074G= , CM000685.1:g.37587074G= GRCh37
NC_000023.9:g.37472013G= NCBI36
NG_007473.1:g.46962G=
NG_007473.3:g.46942G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378616.5:c.694G= MANE Select ENSP00000367879.3:p.Val232=
ENST00000378616.3:c.694G= ENSP00000367879.3:p.Val232=
ENST00000465127.1:c.171+301821G= ENSP00000417050.1:n.171+301821G=
NM_021083.2:c.694G= NP_066569.1:p.Val232=
NM_021083.4:c.694G= MANE Select NP_066569.1:p.Val232=