Canonical Allele Identifier: CA507555537

Gene: BCKDHA

Linked Data

• MyVariant Identifiers: chr19:g.41916691C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41410786C>T , CM000681.2:g.41410786C>T	GRCh38
NC_000019.9:g.41916691C>T , CM000681.1:g.41916691C>T	GRCh37
NC_000019.8:g.46608531C>T	NCBI36
NG_013004.1:g.17998C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269980.7:c.258C>T MANE Select	ENSP00000269980.2:p.Gly86=
ENST00000269980.6:c.258C>T	ENSP00000269980.2:p.Gly86=
ENST00000457836.6:c.192C>T	ENSP00000416000.2:p.Gly64=
ENST00000538423.5:n.278C>T
ENST00000540732.3:c.360C>T	ENSP00000443246.1:p.Gly120=
ENST00000541315.1:c.65C>T
ENST00000542943.5:c.258C>T	ENSP00000440345.1:p.Gly86=
ENST00000595085.5:c.258C>T	ENSP00000471150.2:p.Gly86=
ENST00000604424.1:n.500C>T
NM_000709.3:c.258C>T	NP_000700.1:p.Gly86=
NM_001164783.1:c.258C>T	NP_001158255.1:p.Gly86=
NM_000709.4:c.258C>T MANE Select	NP_000700.1:p.Gly86=
NM_001164783.2:c.258C>T	NP_001158255.1:p.Gly86=