Canonical Allele Identifier: CA412974477
Gene: XK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37727930A>T , CM000685.2:g.37727930A>T GRCh38
NC_000023.10:g.37587183A>T , CM000685.1:g.37587183A>T GRCh37
NC_000023.9:g.37472122A>T NCBI36
NG_007473.1:g.47071A>T
NG_007473.3:g.47051A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378616.5:c.803A>T MANE Select ENSP00000367879.3:p.Glu268Val
ENST00000378616.3:c.803A>T ENSP00000367879.3:p.Glu268Val
ENST00000465127.1:c.171+301930A>T ENSP00000417050.1:n.171+301930A>T
NM_021083.2:c.803A>T NP_066569.1:p.Glu268Val
NM_021083.4:c.803A>T MANE Select NP_066569.1:p.Glu268Val