Canonical Allele Identifier: CA2424657839
Gene: XK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37727815A= , CM000685.2:g.37727815A= GRCh38
NC_000023.10:g.37587068A= , CM000685.1:g.37587068A= GRCh37
NC_000023.9:g.37472007A= NCBI36
NG_007473.1:g.46956A=
NG_007473.3:g.46936A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378616.5:c.688A= MANE Select ENSP00000367879.3:p.Thr230=
ENST00000378616.3:c.688A= ENSP00000367879.3:p.Thr230=
ENST00000465127.1:c.171+301815A= ENSP00000417050.1:n.171+301815A=
NM_021083.2:c.688A= NP_066569.1:p.Thr230=
NM_021083.4:c.688A= MANE Select NP_066569.1:p.Thr230=