Canonical Allele Identifier: CA2424657841
Gene: XK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37727820C= , CM000685.2:g.37727820C= GRCh38
NC_000023.10:g.37587073C= , CM000685.1:g.37587073C= GRCh37
NC_000023.9:g.37472012C= NCBI36
NG_007473.1:g.46961C=
NG_007473.3:g.46941C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378616.5:c.693C= MANE Select ENSP00000367879.3:p.Ser231=
ENST00000378616.3:c.693C= ENSP00000367879.3:p.Ser231=
ENST00000465127.1:c.171+301820C= ENSP00000417050.1:n.171+301820C=
NM_021083.2:c.693C= NP_066569.1:p.Ser231=
NM_021083.4:c.693C= MANE Select NP_066569.1:p.Ser231=