Canonical Allele Identifier: CA2585306884
Gene: BCKDHA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41411102_41411103del , CM000681.2:g.41411102_41411103del GRCh38
NC_000019.9:g.41917007_41917008del , CM000681.1:g.41917007_41917008del GRCh37
NC_000019.8:g.46608847_46608848del NCBI36
NG_013004.1:g.18314_18315del

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.375+93_375+94del MANE Select ENSP00000269980.2:n.375+93_375+94del
ENST00000269980.6:c.375+93_375+94del ENSP00000269980.2:n.375+93_375+94del
ENST00000457836.6:c.309+93_309+94del ENSP00000416000.2:n.309+93_309+94del
ENST00000538423.5:n.501+93_501+94del
ENST00000540732.3:c.477+93_477+94del ENSP00000443246.1:n.477+93_477+94del
ENST00000541315.1:c.182+93_182+94del
ENST00000542943.5:c.288+286_288+287del ENSP00000440345.1:n.288+286_288+287del
ENST00000595085.5:c.375+93_375+94del ENSP00000471150.2:n.375+93_375+94del
NM_000709.3:c.375+93_375+94del NP_000700.1:n.375+93_375+94del
NM_001164783.1:c.375+93_375+94del NP_001158255.1:n.375+93_375+94del
NM_000709.4:c.375+93_375+94del MANE Select NP_000700.1:n.375+93_375+94del
NM_001164783.2:c.375+93_375+94del NP_001158255.1:n.375+93_375+94del