Canonical Allele Identifier: CA412974059
Gene: XK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37727819C>T , CM000685.2:g.37727819C>T GRCh38
NC_000023.10:g.37587072C>T , CM000685.1:g.37587072C>T GRCh37
NC_000023.9:g.37472011C>T NCBI36
NG_007473.1:g.46960C>T
NG_007473.3:g.46940C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378616.5:c.692C>T MANE Select ENSP00000367879.3:p.Ser231Phe
ENST00000378616.3:c.692C>T ENSP00000367879.3:p.Ser231Phe
ENST00000465127.1:c.171+301819C>T ENSP00000417050.1:n.171+301819C>T
NM_021083.2:c.692C>T NP_066569.1:p.Ser231Phe
NM_021083.4:c.692C>T MANE Select NP_066569.1:p.Ser231Phe