Canonical Allele Identifier: CA406015601

Gene: BCKDHA

Linked Data

• MyVariant Identifiers: chr19:g.41930467T>C (hg19) ; chr19:g.41424562T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41424562T>C , CM000681.2:g.41424562T>C	GRCh38
NC_000019.9:g.41930467T>C , CM000681.1:g.41930467T>C	GRCh37
NC_000019.8:g.46622307T>C	NCBI36
NG_013004.1:g.31774T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269980.7:c.1292T>C MANE Select	ENSP00000269980.2:p.Leu431Pro
ENST00000269980.6:c.1292T>C	ENSP00000269980.2:p.Leu431Pro
ENST00000457836.6:c.1301T>C	ENSP00000416000.2:p.Leu434Pro
ENST00000540732.3:c.1394T>C	ENSP00000443246.1:p.Leu465Pro
ENST00000544905.1:c.122T>C
ENST00000595085.5:c.922+1865T>C	ENSP00000471150.2:n.922+1865T>C
NM_000709.3:c.1292T>C	NP_000700.1:p.Leu431Pro
NM_001164783.1:c.1289T>C	NP_001158255.1:p.Leu430Pro
NM_000709.4:c.1292T>C MANE Select	NP_000700.1:p.Leu431Pro
NM_001164783.2:c.1289T>C	NP_001158255.1:p.Leu430Pro