Canonical Allele Identifier: CA412974051
Gene: XK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37727818T>C , CM000685.2:g.37727818T>C GRCh38
NC_000023.10:g.37587071T>C , CM000685.1:g.37587071T>C GRCh37
NC_000023.9:g.37472010T>C NCBI36
NG_007473.1:g.46959T>C
NG_007473.3:g.46939T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378616.5:c.691T>C MANE Select ENSP00000367879.3:p.Ser231Pro
ENST00000378616.3:c.691T>C ENSP00000367879.3:p.Ser231Pro
ENST00000465127.1:c.171+301818T>C ENSP00000417050.1:n.171+301818T>C
NM_021083.2:c.691T>C NP_066569.1:p.Ser231Pro
NM_021083.4:c.691T>C MANE Select NP_066569.1:p.Ser231Pro