Canonical Allele Identifier: CA412974257
Gene: XK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37727866A>G , CM000685.2:g.37727866A>G GRCh38
NC_000023.10:g.37587119A>G , CM000685.1:g.37587119A>G GRCh37
NC_000023.9:g.37472058A>G NCBI36
NG_007473.1:g.47007A>G
NG_007473.3:g.46987A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378616.5:c.739A>G MANE Select ENSP00000367879.3:p.Ser247Gly
ENST00000378616.3:c.739A>G ENSP00000367879.3:p.Ser247Gly
ENST00000465127.1:c.171+301866A>G ENSP00000417050.1:n.171+301866A>G
NM_021083.2:c.739A>G NP_066569.1:p.Ser247Gly
NM_021083.4:c.739A>G MANE Select NP_066569.1:p.Ser247Gly