Canonical Allele Identifier: CA10383574
Gene: XK HGNC NCBI

Linked Data

dbSNP Id: rs782587141
gnomAD v3: X-37727838-G-A
gnomAD v4: X-37727838-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37727838G>A , CM000685.2:g.37727838G>A GRCh38
NC_000023.10:g.37587091G>A , CM000685.1:g.37587091G>A GRCh37
NC_000023.9:g.37472030G>A NCBI36
NG_007473.1:g.46979G>A
NG_007473.3:g.46959G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378616.5:c.711G>A MANE Select ENSP00000367879.3:p.Val237=
ENST00000378616.3:c.711G>A ENSP00000367879.3:p.Val237=
ENST00000465127.1:c.171+301838G>A ENSP00000417050.1:n.171+301838G>A
NM_021083.2:c.711G>A NP_066569.1:p.Val237=
NM_021083.4:c.711G>A MANE Select NP_066569.1:p.Val237=