Canonical Allele Identifier: CA406004676

Gene: BCKDHA

Linked Data

• MyVariant Identifiers: chr19:g.41916611G>T (hg19) ; chr19:g.41410706G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41410706G>T , CM000681.2:g.41410706G>T	GRCh38
NC_000019.9:g.41916611G>T , CM000681.1:g.41916611G>T	GRCh37
NC_000019.8:g.46608451G>T	NCBI36
NG_013004.1:g.17918G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269980.7:c.178G>T MANE Select	ENSP00000269980.2:p.Glu60Ter
ENST00000269980.6:c.178G>T	ENSP00000269980.2:p.Glu60Ter
ENST00000457836.6:c.112G>T	ENSP00000416000.2:p.Glu38Ter
ENST00000538423.5:n.198G>T
ENST00000540732.3:c.280G>T	ENSP00000443246.1:p.Glu94Ter
ENST00000542943.5:c.178G>T	ENSP00000440345.1:p.Glu60Ter
ENST00000595085.5:c.178G>T	ENSP00000471150.2:p.Glu60Ter
ENST00000604424.1:n.420G>T
NM_000709.3:c.178G>T	NP_000700.1:p.Glu60Ter
NM_001164783.1:c.178G>T	NP_001158255.1:p.Glu60Ter
NM_000709.4:c.178G>T MANE Select	NP_000700.1:p.Glu60Ter
NM_001164783.2:c.178G>T	NP_001158255.1:p.Glu60Ter