Canonical Allele Identifier: CA2585308088

Gene: BCKDHA

Linked Data

• gnomAD v4: 19-41422543-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41422544dup , CM000681.2:g.41422544dup	GRCh38
NC_000019.9:g.41928449dup , CM000681.1:g.41928449dup	GRCh37
NC_000019.8:g.46620289dup	NCBI36
NG_013004.1:g.29756dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269980.7:c.854-85dup MANE Select	ENSP00000269980.2:n.854-85dup
ENST00000269980.6:c.854-85dup	ENSP00000269980.2:n.854-85dup
ENST00000457836.6:c.788-85dup	ENSP00000416000.2:n.788-85dup
ENST00000535632.5:n.483-85dup
ENST00000540732.3:c.956-85dup	ENSP00000443246.1:n.956-85dup
ENST00000542943.5:c.767-85dup	ENSP00000440345.1:n.767-85dup
ENST00000545787.1:n.482-85dup
ENST00000595085.5:c.854-85dup	ENSP00000471150.2:n.854-85dup
NM_000709.3:c.854-85dup	NP_000700.1:n.854-85dup
NM_001164783.1:c.854-88dup	NP_001158255.1:n.854-88dup
NM_000709.4:c.854-85dup MANE Select	NP_000700.1:n.854-85dup
NM_001164783.2:c.854-88dup	NP_001158255.1:n.854-88dup