Canonical Allele Identifier: CA406005517

Gene: BCKDHA

Linked Data

• MyVariant Identifiers: chr19:g.41916856A>T (hg19) ; chr19:g.41410951A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41410951A>T , CM000681.2:g.41410951A>T	GRCh38
NC_000019.9:g.41916856A>T , CM000681.1:g.41916856A>T	GRCh37
NC_000019.8:g.46608696A>T	NCBI36
NG_013004.1:g.18163A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269980.7:c.317A>T MANE Select	ENSP00000269980.2:p.Tyr106Phe
ENST00000269980.6:c.317A>T	ENSP00000269980.2:p.Tyr106Phe
ENST00000457836.6:c.251A>T	ENSP00000416000.2:p.Tyr84Phe
ENST00000538423.5:n.443A>T
ENST00000540732.3:c.419A>T	ENSP00000443246.1:p.Tyr140Phe
ENST00000541315.1:c.124A>T
ENST00000542943.5:c.288+135A>T	ENSP00000440345.1:n.288+135A>T
ENST00000595085.5:c.317A>T	ENSP00000471150.2:p.Tyr106Phe
NM_000709.3:c.317A>T	NP_000700.1:p.Tyr106Phe
NM_001164783.1:c.317A>T	NP_001158255.1:p.Tyr106Phe
NM_000709.4:c.317A>T MANE Select	NP_000700.1:p.Tyr106Phe
NM_001164783.2:c.317A>T	NP_001158255.1:p.Tyr106Phe