Canonical Allele Identifier: CA406013443

Gene: BCKDHA

Linked Data

• MyVariant Identifiers: chr19:g.41928624G>C (hg19) ; chr19:g.41422719G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41422719G>C , CM000681.2:g.41422719G>C	GRCh38
NC_000019.9:g.41928624G>C , CM000681.1:g.41928624G>C	GRCh37
NC_000019.8:g.46620464G>C	NCBI36
NG_013004.1:g.29931G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269980.7:c.944G>C MANE Select	ENSP00000269980.2:p.Arg315Pro
ENST00000269980.6:c.944G>C	ENSP00000269980.2:p.Arg315Pro
ENST00000457836.6:c.878G>C	ENSP00000416000.2:p.Arg293Pro
ENST00000535632.5:n.573G>C
ENST00000540732.3:c.1046G>C	ENSP00000443246.1:p.Arg349Pro
ENST00000542943.5:c.857G>C	ENSP00000440345.1:p.Arg286Pro
ENST00000545787.1:n.572G>C
ENST00000595085.5:c.922+22G>C	ENSP00000471150.2:n.922+22G>C
NM_000709.3:c.944G>C	NP_000700.1:p.Arg315Pro
NM_001164783.1:c.941G>C	NP_001158255.1:p.Arg314Pro
NM_000709.4:c.944G>C MANE Select	NP_000700.1:p.Arg315Pro
NM_001164783.2:c.941G>C	NP_001158255.1:p.Arg314Pro