Canonical Allele Identifier: CA2585307954

Gene: BCKDHA

Linked Data

• gnomAD v4: 19-41422092-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41422092T>C , CM000681.2:g.41422092T>C	GRCh38
NC_000019.9:g.41927997T>C , CM000681.1:g.41927997T>C	GRCh37
NC_000019.8:g.46619837T>C	NCBI36
NG_013004.1:g.29304T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000269980.7:c.647-72T>C MANE Select	ENSP00000269980.2:n.647-72T>C
ENST00000269980.6:c.647-72T>C	ENSP00000269980.2:n.647-72T>C
ENST00000457836.6:c.581-72T>C	ENSP00000416000.2:n.581-72T>C
ENST00000535632.5:n.276-72T>C
ENST00000538423.5:n.773-72T>C
ENST00000540732.3:c.749-72T>C	ENSP00000443246.1:n.749-72T>C
ENST00000541315.1:c.547-72T>C
ENST00000542943.5:c.560-72T>C	ENSP00000440345.1:n.560-72T>C
ENST00000545787.1:n.275-72T>C
ENST00000595085.5:c.647-72T>C	ENSP00000471150.2:n.647-72T>C
NM_000709.3:c.647-72T>C	NP_000700.1:n.647-72T>C
NM_001164783.1:c.647-72T>C	NP_001158255.1:n.647-72T>C
NM_000709.4:c.647-72T>C MANE Select	NP_000700.1:n.647-72T>C
NM_001164783.2:c.647-72T>C	NP_001158255.1:n.647-72T>C