Canonical Allele Identifier: CA876055142
Gene: DGKK HGNC NCBI

Linked Data

dbSNP Id: rs1329013596
MyVariant Identifiers: chrX:g.50459811T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.50459811T>C , CM000685.2:g.50459811T>C GRCh38
NC_000023.10:g.50202809T>C , CM000685.1:g.50202809T>C GRCh37
NC_000023.9:g.50219549T>C NCBI36
NG_033143.2:g.15912A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000611977.2:c.645+10223A>G MANE Select ENSP00000477515.1:n.645+10223A>G
ENST00000611977.1:c.645+10223A>G ENSP00000477515.1:n.645+10223A>G
NM_001013742.3:c.645+10223A>G NP_001013764.1:n.645+10223A>G
XM_017029268.2:c.645+10223A>G XP_016884757.1:n.645+10223A>G
NM_001013742.4:c.645+10223A>G MANE Select NP_001013764.1:n.645+10223A>G
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