Canonical Allele Identifier: CA412974037

Gene: XK

Linked Data

• dbSNP Id: rs1928007793
• MyVariant Identifiers: chrX:g.37587068A>G (hg19) ; chrX:g.37727815A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37727815A>G , CM000685.2:g.37727815A>G	GRCh38
NC_000023.10:g.37587068A>G , CM000685.1:g.37587068A>G	GRCh37
NC_000023.9:g.37472007A>G	NCBI36
NG_007473.1:g.46956A>G
NG_007473.3:g.46936A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378616.5:c.688A>G MANE Select	ENSP00000367879.3:p.Thr230Ala
ENST00000378616.3:c.688A>G	ENSP00000367879.3:p.Thr230Ala
ENST00000465127.1:c.171+301815A>G	ENSP00000417050.1:n.171+301815A>G
NM_021083.2:c.688A>G	NP_066569.1:p.Thr230Ala
NM_021083.4:c.688A>G MANE Select	NP_066569.1:p.Thr230Ala