Canonical Allele Identifier: CA2814427366
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41421966G>C , CM000681.2:g.41421966G>C GRCh38
NC_000019.9:g.41927871G>C , CM000681.1:g.41927871G>C GRCh37
NC_000019.8:g.46619711G>C NCBI36
NG_013004.1:g.29178G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.647-198G>C MANE Select ENSP00000269980.2:n.647-198G>C
ENST00000269980.6:c.647-198G>C ENSP00000269980.2:n.647-198G>C
ENST00000457836.6:c.581-198G>C ENSP00000416000.2:n.581-198G>C
ENST00000535632.5:n.276-198G>C
ENST00000538423.5:n.773-198G>C
ENST00000540732.3:c.749-198G>C ENSP00000443246.1:n.749-198G>C
ENST00000541315.1:c.547-198G>C
ENST00000542943.5:c.560-198G>C ENSP00000440345.1:n.560-198G>C
ENST00000545787.1:n.275-198G>C
ENST00000595085.5:c.647-198G>C ENSP00000471150.2:n.647-198G>C
NM_000709.3:c.647-198G>C NP_000700.1:n.647-198G>C
NM_001164783.1:c.647-198G>C NP_001158255.1:n.647-198G>C
NM_000709.4:c.647-198G>C MANE Select NP_000700.1:n.647-198G>C
NM_001164783.2:c.647-198G>C NP_001158255.1:n.647-198G>C