Canonical Allele Identifier: CA995976596

Gene: BCKDHA

Linked Data

• dbSNP Id: rs561161412
• gnomAD v3: 19-41422483-G-C
• gnomAD v4: 19-41422483-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41422483G>C , CM000681.2:g.41422483G>C	GRCh38
NC_000019.9:g.41928388G>C , CM000681.1:g.41928388G>C	GRCh37
NC_000019.8:g.46620228G>C	NCBI36
NG_013004.1:g.29695G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269980.7:c.853+113G>C MANE Select	ENSP00000269980.2:n.853+113G>C
ENST00000269980.6:c.853+113G>C	ENSP00000269980.2:n.853+113G>C
ENST00000457836.6:c.787+113G>C	ENSP00000416000.2:n.787+113G>C
ENST00000535632.5:n.482+113G>C
ENST00000540732.3:c.955+113G>C	ENSP00000443246.1:n.955+113G>C
ENST00000542943.5:c.766+113G>C	ENSP00000440345.1:n.766+113G>C
ENST00000545787.1:n.481+113G>C
ENST00000595085.5:c.853+113G>C	ENSP00000471150.2:n.853+113G>C
NM_000709.3:c.853+113G>C	NP_000700.1:n.853+113G>C
NM_001164783.1:c.853+113G>C	NP_001158255.1:n.853+113G>C
NM_000709.4:c.853+113G>C MANE Select	NP_000700.1:n.853+113G>C
NM_001164783.2:c.853+113G>C	NP_001158255.1:n.853+113G>C