Canonical Allele Identifier: CA507690619

Gene: BCKDHA

Linked Data

• MyVariant Identifiers: chr19:g.41928544C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41422639C>T , CM000681.2:g.41422639C>T	GRCh38
NC_000019.9:g.41928544C>T , CM000681.1:g.41928544C>T	GRCh37
NC_000019.8:g.46620384C>T	NCBI36
NG_013004.1:g.29851C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000269980.7:c.864C>T MANE Select	ENSP00000269980.2:p.Gly288=
ENST00000269980.6:c.864C>T	ENSP00000269980.2:p.Gly288=
ENST00000457836.6:c.798C>T	ENSP00000416000.2:p.Gly266=
ENST00000535632.5:n.493C>T
ENST00000540732.3:c.966C>T	ENSP00000443246.1:p.Gly322=
ENST00000542943.5:c.777C>T	ENSP00000440345.1:p.Gly259=
ENST00000545787.1:n.492C>T
ENST00000595085.5:c.864C>T	ENSP00000471150.2:p.Gly288=
NM_000709.3:c.864C>T	NP_000700.1:p.Gly288=
NM_001164783.1:c.861C>T	NP_001158255.1:p.Gly287=
NM_000709.4:c.864C>T MANE Select	NP_000700.1:p.Gly288=
NM_001164783.2:c.861C>T	NP_001158255.1:p.Gly287=