Canonical Allele Identifier: CA392862428
Gene: KBTBD13 HGNC NCBI

Linked Data

COSMIC: COSM5034348
MyVariant Identifiers: chr15:g.65369848A>C (hg19) chr15:g.65077510A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.65077510A>C , CM000677.2:g.65077510A>C GRCh38
NC_000015.9:g.65369848A>C , CM000677.1:g.65369848A>C GRCh37
NC_000015.8:g.63156901A>C NCBI36
NG_021411.1:g.5695A>C , LRG_682:g.5695A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000432196.5:c.695A>C MANE Select ENSP00000388723.2:p.Asp232Ala
ENST00000432196.3:c.695A>C ENSP00000388723.2:p.Asp232Ala
NM_001101362.2:c.695A>C , LRG_682t1:c.695A>C NP_001094832.1:p.Asp232Ala
NM_001101362.3:c.695A>C MANE Select NP_001094832.1:p.Asp232Ala
Search 100 bp 5'
Search 100 bp 3'