Canonical Allele Identifier: CA412974702
Gene: XK HGNC NCBI

Linked Data

gnomAD v4: X-37728030-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37728030A>C , CM000685.2:g.37728030A>C GRCh38
NC_000023.10:g.37587283A>C , CM000685.1:g.37587283A>C GRCh37
NC_000023.9:g.37472222A>C NCBI36
NG_007473.1:g.47171A>C
NG_007473.3:g.47151A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378616.5:c.903A>C MANE Select ENSP00000367879.3:p.Lys301Asn
ENST00000378616.3:c.903A>C ENSP00000367879.3:p.Lys301Asn
ENST00000465127.1:c.171+302030A>C ENSP00000417050.1:n.171+302030A>C
NM_021083.2:c.903A>C NP_066569.1:p.Lys301Asn
NM_021083.4:c.903A>C MANE Select NP_066569.1:p.Lys301Asn