Canonical Allele Identifier: CA406012739

Gene: BCKDHA

Linked Data

• COSMIC: COSM4078534
• MyVariant Identifiers: chr19:g.41928113G>A (hg19) ; chr19:g.41422208G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41422208G>A , CM000681.2:g.41422208G>A	GRCh38
NC_000019.9:g.41928113G>A , CM000681.1:g.41928113G>A	GRCh37
NC_000019.8:g.46619953G>A	NCBI36
NG_013004.1:g.29420G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269980.7:c.691G>A MANE Select	ENSP00000269980.2:p.Val231Ile
ENST00000269980.6:c.691G>A	ENSP00000269980.2:p.Val231Ile
ENST00000457836.6:c.625G>A	ENSP00000416000.2:p.Val209Ile
ENST00000535632.5:n.320G>A
ENST00000540732.3:c.793G>A	ENSP00000443246.1:p.Val265Ile
ENST00000541315.1:c.591G>A
ENST00000542943.5:c.604G>A	ENSP00000440345.1:p.Val202Ile
ENST00000545787.1:n.319G>A
ENST00000595085.5:c.691G>A	ENSP00000471150.2:p.Val231Ile
NM_000709.3:c.691G>A	NP_000700.1:p.Val231Ile
NM_001164783.1:c.691G>A	NP_001158255.1:p.Val231Ile
NM_000709.4:c.691G>A MANE Select	NP_000700.1:p.Val231Ile
NM_001164783.2:c.691G>A	NP_001158255.1:p.Val231Ile