Canonical Allele Identifier: CA406013764

Gene: BCKDHA

Linked Data

• MyVariant Identifiers: chr19:g.41928915C>G (hg19) ; chr19:g.41423010C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41423010C>G , CM000681.2:g.41423010C>G	GRCh38
NC_000019.9:g.41928915C>G , CM000681.1:g.41928915C>G	GRCh37
NC_000019.8:g.46620755C>G	NCBI36
NG_013004.1:g.30222C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269980.7:c.1008C>G MANE Select	ENSP00000269980.2:p.His336Gln
ENST00000269980.6:c.1008C>G	ENSP00000269980.2:p.His336Gln
ENST00000457836.6:c.1017C>G	ENSP00000416000.2:p.His339Gln
ENST00000540732.3:c.1110C>G	ENSP00000443246.1:p.His370Gln
ENST00000542943.5:c.921C>G	ENSP00000440345.1:p.His307Gln
ENST00000595085.5:c.922+313C>G	ENSP00000471150.2:n.922+313C>G
NM_000709.3:c.1008C>G	NP_000700.1:p.His336Gln
NM_001164783.1:c.1005C>G	NP_001158255.1:p.His335Gln
NM_000709.4:c.1008C>G MANE Select	NP_000700.1:p.His336Gln
NM_001164783.2:c.1005C>G	NP_001158255.1:p.His335Gln