Canonical Allele Identifier: CA2336453993
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41411060C= , CM000681.2:g.41411060C= GRCh38
NC_000019.9:g.41916965C= , CM000681.1:g.41916965C= GRCh37
NC_000019.8:g.46608805C= NCBI36
NG_013004.1:g.18272C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.375+51C= MANE Select ENSP00000269980.2:n.375+51C=
ENST00000269980.6:c.375+51C= ENSP00000269980.2:n.375+51C=
ENST00000457836.6:c.309+51C= ENSP00000416000.2:n.309+51C=
ENST00000538423.5:n.501+51C=
ENST00000540732.3:c.477+51C= ENSP00000443246.1:n.477+51C=
ENST00000541315.1:c.182+51C=
ENST00000542943.5:c.288+244C= ENSP00000440345.1:n.288+244C=
ENST00000595085.5:c.375+51C= ENSP00000471150.2:n.375+51C=
NM_000709.3:c.375+51C= NP_000700.1:n.375+51C=
NM_001164783.1:c.375+51C= NP_001158255.1:n.375+51C=
NM_000709.4:c.375+51C= MANE Select NP_000700.1:n.375+51C=
NM_001164783.2:c.375+51C= NP_001158255.1:n.375+51C=