Canonical Allele Identifier: CA308524618

Gene: BCKDHA

Linked Data

• dbSNP Id: rs9710116
• MyVariant Identifiers: chr19:g.41928419T>C (hg19) ; chr19:g.41422514T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41422514T>C , CM000681.2:g.41422514T>C	GRCh38
NC_000019.9:g.41928419T>C , CM000681.1:g.41928419T>C	GRCh37
NC_000019.8:g.46620259T>C	NCBI36
NG_013004.1:g.29726T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269980.7:c.854-115T>C MANE Select	ENSP00000269980.2:n.854-115T>C
ENST00000269980.6:c.854-115T>C	ENSP00000269980.2:n.854-115T>C
ENST00000457836.6:c.788-115T>C	ENSP00000416000.2:n.788-115T>C
ENST00000535632.5:n.483-115T>C
ENST00000540732.3:c.956-115T>C	ENSP00000443246.1:n.956-115T>C
ENST00000542943.5:c.767-115T>C	ENSP00000440345.1:n.767-115T>C
ENST00000545787.1:n.482-115T>C
ENST00000595085.5:c.854-115T>C	ENSP00000471150.2:n.854-115T>C
NM_000709.3:c.854-115T>C	NP_000700.1:n.854-115T>C
NM_001164783.1:c.854-118T>C	NP_001158255.1:n.854-118T>C
NM_000709.4:c.854-115T>C MANE Select	NP_000700.1:n.854-115T>C
NM_001164783.2:c.854-118T>C	NP_001158255.1:n.854-118T>C