Canonical Allele Identifier: CA412974709

Gene: XK

Linked Data

• gnomAD v4: X-37728033-T-G
• MyVariant Identifiers: chrX:g.37587286T>G (hg19) ; chrX:g.37728033T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.37728033T>G , CM000685.2:g.37728033T>G	GRCh38
NC_000023.10:g.37587286T>G , CM000685.1:g.37587286T>G	GRCh37
NC_000023.9:g.37472225T>G	NCBI36
NG_007473.1:g.47174T>G
NG_007473.3:g.47154T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378616.5:c.906T>G MANE Select	ENSP00000367879.3:p.Ile302Met
ENST00000378616.3:c.906T>G	ENSP00000367879.3:p.Ile302Met
ENST00000465127.1:c.171+302033T>G	ENSP00000417050.1:n.171+302033T>G
NM_021083.2:c.906T>G	NP_066569.1:p.Ile302Met
NM_021083.4:c.906T>G MANE Select	NP_066569.1:p.Ile302Met