Canonical Allele Identifier: CA412974695
Gene: XK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37728028A>C , CM000685.2:g.37728028A>C GRCh38
NC_000023.10:g.37587281A>C , CM000685.1:g.37587281A>C GRCh37
NC_000023.9:g.37472220A>C NCBI36
NG_007473.1:g.47169A>C
NG_007473.3:g.47149A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378616.5:c.901A>C MANE Select ENSP00000367879.3:p.Lys301Gln
ENST00000378616.3:c.901A>C ENSP00000367879.3:p.Lys301Gln
ENST00000465127.1:c.171+302028A>C ENSP00000417050.1:n.171+302028A>C
NM_021083.2:c.901A>C NP_066569.1:p.Lys301Gln
NM_021083.4:c.901A>C MANE Select NP_066569.1:p.Lys301Gln