Canonical Allele Identifier: CA406013514

Gene: BCKDHA

Linked Data

• MyVariant Identifiers: chr19:g.41928660A>C (hg19) ; chr19:g.41422755A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41422755A>C , CM000681.2:g.41422755A>C	GRCh38
NC_000019.9:g.41928660A>C , CM000681.1:g.41928660A>C	GRCh37
NC_000019.8:g.46620500A>C	NCBI36
NG_013004.1:g.29967A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269980.7:c.980A>C MANE Select	ENSP00000269980.2:p.Glu327Ala
ENST00000269980.6:c.980A>C	ENSP00000269980.2:p.Glu327Ala
ENST00000457836.6:c.914A>C	ENSP00000416000.2:p.Glu305Ala
ENST00000535632.5:n.609A>C
ENST00000540732.3:c.1082A>C	ENSP00000443246.1:p.Glu361Ala
ENST00000542943.5:c.893A>C	ENSP00000440345.1:p.Glu298Ala
ENST00000595085.5:c.922+58A>C	ENSP00000471150.2:n.922+58A>C
NM_000709.3:c.980A>C	NP_000700.1:p.Glu327Ala
NM_001164783.1:c.977A>C	NP_001158255.1:p.Glu326Ala
NM_000709.4:c.980A>C MANE Select	NP_000700.1:p.Glu327Ala
NM_001164783.2:c.977A>C	NP_001158255.1:p.Glu326Ala