Canonical Allele Identifier: CA2693424520
Gene: XK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37727817del , CM000685.2:g.37727817del GRCh38
NC_000023.10:g.37587070del , CM000685.1:g.37587070del GRCh37
NC_000023.9:g.37472009del NCBI36
NG_007473.1:g.46958del
NG_007473.3:g.46938del

Transcript Alleles

HGVS Amino-acid Change
ENST00000378616.5:c.690del MANE Select ENSP00000367879.3:p.Ser231ProfsTer3
ENST00000378616.3:c.690del ENSP00000367879.3:p.Ser231ProfsTer3
ENST00000465127.1:c.171+301817del ENSP00000417050.1:n.171+301817del
NM_021083.2:c.690del NP_066569.1:p.Ser231ProfsTer3
NM_021083.4:c.690del MANE Select NP_066569.1:p.Ser231ProfsTer3