Canonical Allele Identifier: CA2576793760
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41411053A>T , CM000681.2:g.41411053A>T GRCh38
NC_000019.9:g.41916958A>T , CM000681.1:g.41916958A>T GRCh37
NC_000019.8:g.46608798A>T NCBI36
NG_013004.1:g.18265A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.375+44A>T MANE Select ENSP00000269980.2:n.375+44A>T
ENST00000269980.6:c.375+44A>T ENSP00000269980.2:n.375+44A>T
ENST00000457836.6:c.309+44A>T ENSP00000416000.2:n.309+44A>T
ENST00000538423.5:n.501+44A>T
ENST00000540732.3:c.477+44A>T ENSP00000443246.1:n.477+44A>T
ENST00000541315.1:c.182+44A>T
ENST00000542943.5:c.288+237A>T ENSP00000440345.1:n.288+237A>T
ENST00000595085.5:c.375+44A>T ENSP00000471150.2:n.375+44A>T
NM_000709.3:c.375+44A>T NP_000700.1:n.375+44A>T
NM_001164783.1:c.375+44A>T NP_001158255.1:n.375+44A>T
NM_000709.4:c.375+44A>T MANE Select NP_000700.1:n.375+44A>T
NM_001164783.2:c.375+44A>T NP_001158255.1:n.375+44A>T