Canonical Allele Identifier: CA2183439969
Gene: KBTBD13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.65077421C= , CM000677.2:g.65077421C= GRCh38
NC_000015.9:g.65369759C= , CM000677.1:g.65369759C= GRCh37
NC_000015.8:g.63156812C= NCBI36
NG_021411.1:g.5606C= , LRG_682:g.5606C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000432196.5:c.606C= MANE Select ENSP00000388723.2:p.Ala202=
ENST00000432196.3:c.606C= ENSP00000388723.2:p.Ala202=
NM_001101362.2:c.606C= , LRG_682t1:c.606C= NP_001094832.1:p.Ala202=
NM_001101362.3:c.606C= MANE Select NP_001094832.1:p.Ala202=