Canonical Allele Identifier: CA2336459188
Gene: BCKDHA HGNC NCBI

Linked Data

dbSNP Id: rs1185440873

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41422606C>G , CM000681.2:g.41422606C>G GRCh38
NC_000019.9:g.41928511C>G , CM000681.1:g.41928511C>G GRCh37
NC_000019.8:g.46620351C>G NCBI36
NG_013004.1:g.29818C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.854-23C>G MANE Select ENSP00000269980.2:n.854-23C>G
ENST00000269980.6:c.854-23C>G ENSP00000269980.2:n.854-23C>G
ENST00000457836.6:c.788-23C>G ENSP00000416000.2:n.788-23C>G
ENST00000535632.5:n.483-23C>G
ENST00000540732.3:c.956-23C>G ENSP00000443246.1:n.956-23C>G
ENST00000542943.5:c.767-23C>G ENSP00000440345.1:n.767-23C>G
ENST00000545787.1:n.482-23C>G
ENST00000595085.5:c.854-23C>G ENSP00000471150.2:n.854-23C>G
NM_000709.3:c.854-23C>G NP_000700.1:n.854-23C>G
NM_001164783.1:c.854-26C>G NP_001158255.1:n.854-26C>G
NM_000709.4:c.854-23C>G MANE Select NP_000700.1:n.854-23C>G
NM_001164783.2:c.854-26C>G NP_001158255.1:n.854-26C>G