Canonical Allele Identifier: CA406015488

Gene: BCKDHA

Linked Data

• MyVariant Identifiers: chr19:g.41930440A>T (hg19) ; chr19:g.41424535A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41424535A>T , CM000681.2:g.41424535A>T	GRCh38
NC_000019.9:g.41930440A>T , CM000681.1:g.41930440A>T	GRCh37
NC_000019.8:g.46622280A>T	NCBI36
NG_013004.1:g.31747A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269980.7:c.1265A>T MANE Select	ENSP00000269980.2:p.Lys422Met
ENST00000269980.6:c.1265A>T	ENSP00000269980.2:p.Lys422Met
ENST00000457836.6:c.1274A>T	ENSP00000416000.2:p.Lys425Met
ENST00000540732.3:c.1367A>T	ENSP00000443246.1:p.Lys456Met
ENST00000544905.1:c.95A>T
ENST00000595085.5:c.922+1838A>T	ENSP00000471150.2:n.922+1838A>T
NM_000709.3:c.1265A>T	NP_000700.1:p.Lys422Met
NM_001164783.1:c.1262A>T	NP_001158255.1:p.Lys421Met
NM_000709.4:c.1265A>T MANE Select	NP_000700.1:p.Lys422Met
NM_001164783.2:c.1262A>T	NP_001158255.1:p.Lys421Met