Canonical Allele Identifier: CA2183440291
Gene: KBTBD13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.65077596T= , CM000677.2:g.65077596T= GRCh38
NC_000015.9:g.65369934T= , CM000677.1:g.65369934T= GRCh37
NC_000015.8:g.63156987T= NCBI36
NG_021411.1:g.5781T= , LRG_682:g.5781T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000432196.5:c.781T= MANE Select ENSP00000388723.2:p.Tyr261=
ENST00000432196.3:c.781T= ENSP00000388723.2:p.Tyr261=
NM_001101362.2:c.781T= , LRG_682t1:c.781T= NP_001094832.1:p.Tyr261=
NM_001101362.3:c.781T= MANE Select NP_001094832.1:p.Tyr261=