Canonical Allele Identifier: CA507690775

Gene: BCKDHA

Linked Data

• MyVariant Identifiers: chr19:g.41928915C>T (hg19)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269980.7:c.1008C>T MANE Select	ENSP00000269980.2:p.His336=
ENST00000269980.6:c.1008C>T	ENSP00000269980.2:p.His336=
ENST00000457836.6:c.1017C>T	ENSP00000416000.2:p.His339=
ENST00000540732.3:c.1110C>T	ENSP00000443246.1:p.His370=
ENST00000542943.5:c.921C>T	ENSP00000440345.1:p.His307=
ENST00000595085.5:c.922+313C>T	ENSP00000471150.2:n.922+313C>T
NM_000709.3:c.1008C>T	NP_000700.1:p.His336=
NM_001164783.1:c.1005C>T	NP_001158255.1:p.His335=
NM_000709.4:c.1008C>T MANE Select	NP_000700.1:p.His336=
NM_001164783.2:c.1005C>T	NP_001158255.1:p.His335=