Canonical Allele Identifier: CA2585308082

Gene: BCKDHA

Linked Data

• gnomAD v4: 19-41422529-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41422529C>G , CM000681.2:g.41422529C>G	GRCh38
NC_000019.9:g.41928434C>G , CM000681.1:g.41928434C>G	GRCh37
NC_000019.8:g.46620274C>G	NCBI36
NG_013004.1:g.29741C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000269980.7:c.854-100C>G MANE Select	ENSP00000269980.2:n.854-100C>G
ENST00000269980.6:c.854-100C>G	ENSP00000269980.2:n.854-100C>G
ENST00000457836.6:c.788-100C>G	ENSP00000416000.2:n.788-100C>G
ENST00000535632.5:n.483-100C>G
ENST00000540732.3:c.956-100C>G	ENSP00000443246.1:n.956-100C>G
ENST00000542943.5:c.767-100C>G	ENSP00000440345.1:n.767-100C>G
ENST00000545787.1:n.482-100C>G
ENST00000595085.5:c.854-100C>G	ENSP00000471150.2:n.854-100C>G
NM_000709.3:c.854-100C>G	NP_000700.1:n.854-100C>G
NM_001164783.1:c.854-103C>G	NP_001158255.1:n.854-103C>G
NM_000709.4:c.854-100C>G MANE Select	NP_000700.1:n.854-100C>G
NM_001164783.2:c.854-103C>G	NP_001158255.1:n.854-103C>G