Canonical Allele Identifier: CA633470337

Gene: BCKDHA

Linked Data

• dbSNP Id: rs1304412476
• gnomAD v2: 19-41928063-C-G
• gnomAD v4: 19-41422158-C-G
• MyVariant Identifiers: chr19:g.41928063C>G (hg19) ; chr19:g.41422158C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41422158C>G , CM000681.2:g.41422158C>G	GRCh38
NC_000019.9:g.41928063C>G , CM000681.1:g.41928063C>G	GRCh37
NC_000019.8:g.46619903C>G	NCBI36
NG_013004.1:g.29370C>G

Transcript Alleles

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