Canonical Allele Identifier: CA2424657876
Gene: XK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37727927T= , CM000685.2:g.37727927T= GRCh38
NC_000023.10:g.37587180T= , CM000685.1:g.37587180T= GRCh37
NC_000023.9:g.37472119T= NCBI36
NG_007473.1:g.47068T=
NG_007473.3:g.47048T=

Transcript Alleles

HGVS Amino-acid change
ENST00000378616.5:c.800T= MANE Select ENSP00000367879.3:p.Ile267=
ENST00000378616.3:c.800T= ENSP00000367879.3:p.Ile267=
ENST00000465127.1:c.171+301927T= ENSP00000417050.1:n.171+301927T=
NM_021083.2:c.800T= NP_066569.1:p.Ile267=
NM_021083.4:c.800T= MANE Select NP_066569.1:p.Ile267=