Canonical Allele Identifier: CA412974471
Gene: XK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37727928A>G , CM000685.2:g.37727928A>G GRCh38
NC_000023.10:g.37587181A>G , CM000685.1:g.37587181A>G GRCh37
NC_000023.9:g.37472120A>G NCBI36
NG_007473.1:g.47069A>G
NG_007473.3:g.47049A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378616.5:c.801A>G MANE Select ENSP00000367879.3:p.Ile267Met
ENST00000378616.3:c.801A>G ENSP00000367879.3:p.Ile267Met
ENST00000465127.1:c.171+301928A>G ENSP00000417050.1:n.171+301928A>G
NM_021083.2:c.801A>G NP_066569.1:p.Ile267Met
NM_021083.4:c.801A>G MANE Select NP_066569.1:p.Ile267Met