Canonical Allele Identifier: CA2576793765
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41411065T>C , CM000681.2:g.41411065T>C GRCh38
NC_000019.9:g.41916970T>C , CM000681.1:g.41916970T>C GRCh37
NC_000019.8:g.46608810T>C NCBI36
NG_013004.1:g.18277T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.375+56T>C MANE Select ENSP00000269980.2:n.375+56T>C
ENST00000269980.6:c.375+56T>C ENSP00000269980.2:n.375+56T>C
ENST00000457836.6:c.309+56T>C ENSP00000416000.2:n.309+56T>C
ENST00000538423.5:n.501+56T>C
ENST00000540732.3:c.477+56T>C ENSP00000443246.1:n.477+56T>C
ENST00000541315.1:c.182+56T>C
ENST00000542943.5:c.288+249T>C ENSP00000440345.1:n.288+249T>C
ENST00000595085.5:c.375+56T>C ENSP00000471150.2:n.375+56T>C
NM_000709.3:c.375+56T>C NP_000700.1:n.375+56T>C
NM_001164783.1:c.375+56T>C NP_001158255.1:n.375+56T>C
NM_000709.4:c.375+56T>C MANE Select NP_000700.1:n.375+56T>C
NM_001164783.2:c.375+56T>C NP_001158255.1:n.375+56T>C