Canonical Allele Identifier: CA2183440266
Gene: KBTBD13 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.65077588G= , CM000677.2:g.65077588G= GRCh38
NC_000015.9:g.65369926G= , CM000677.1:g.65369926G= GRCh37
NC_000015.8:g.63156979G= NCBI36
NG_021411.1:g.5773G= , LRG_682:g.5773G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000432196.5:c.773G= MANE Select ENSP00000388723.2:p.Gly258=
ENST00000432196.3:c.773G= ENSP00000388723.2:p.Gly258=
NM_001101362.2:c.773G= , LRG_682t1:c.773G= NP_001094832.1:p.Gly258=
NM_001101362.3:c.773G= MANE Select NP_001094832.1:p.Gly258=
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