Canonical Allele Identifier: CA2336453991
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41411057C= , CM000681.2:g.41411057C= GRCh38
NC_000019.9:g.41916962C= , CM000681.1:g.41916962C= GRCh37
NC_000019.8:g.46608802C= NCBI36
NG_013004.1:g.18269C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.375+48C= MANE Select ENSP00000269980.2:n.375+48C=
ENST00000269980.6:c.375+48C= ENSP00000269980.2:n.375+48C=
ENST00000457836.6:c.309+48C= ENSP00000416000.2:n.309+48C=
ENST00000538423.5:n.501+48C=
ENST00000540732.3:c.477+48C= ENSP00000443246.1:n.477+48C=
ENST00000541315.1:c.182+48C=
ENST00000542943.5:c.288+241C= ENSP00000440345.1:n.288+241C=
ENST00000595085.5:c.375+48C= ENSP00000471150.2:n.375+48C=
NM_000709.3:c.375+48C= NP_000700.1:n.375+48C=
NM_001164783.1:c.375+48C= NP_001158255.1:n.375+48C=
NM_000709.4:c.375+48C= MANE Select NP_000700.1:n.375+48C=
NM_001164783.2:c.375+48C= NP_001158255.1:n.375+48C=