Canonical Allele Identifier: CA2336454028
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41411120T= , CM000681.2:g.41411120T= GRCh38
NC_000019.9:g.41917025T= , CM000681.1:g.41917025T= GRCh37
NC_000019.8:g.46608865T= NCBI36
NG_013004.1:g.18332T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.375+111T= MANE Select ENSP00000269980.2:n.375+111T=
ENST00000269980.6:c.375+111T= ENSP00000269980.2:n.375+111T=
ENST00000457836.6:c.309+111T= ENSP00000416000.2:n.309+111T=
ENST00000538423.5:n.501+111T=
ENST00000540732.3:c.477+111T= ENSP00000443246.1:n.477+111T=
ENST00000541315.1:c.182+111T=
ENST00000542943.5:c.288+304T= ENSP00000440345.1:n.288+304T=
ENST00000595085.5:c.375+111T= ENSP00000471150.2:n.375+111T=
NM_000709.3:c.375+111T= NP_000700.1:n.375+111T=
NM_001164783.1:c.375+111T= NP_001158255.1:n.375+111T=
NM_000709.4:c.375+111T= MANE Select NP_000700.1:n.375+111T=
NM_001164783.2:c.375+111T= NP_001158255.1:n.375+111T=