Canonical Allele Identifier: CA2336460095
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41424600G= , CM000681.2:g.41424600G= GRCh38
NC_000019.9:g.41930505G= , CM000681.1:g.41930505G= GRCh37
NC_000019.8:g.46622345G= NCBI36
NG_013004.1:g.31812G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.1330G= MANE Select ENSP00000269980.2:p.Asp444=
ENST00000269980.6:c.1330G= ENSP00000269980.2:p.Asp444=
ENST00000457836.6:c.1339G= ENSP00000416000.2:p.Asp447=
ENST00000540732.3:c.1432G= ENSP00000443246.1:p.Asp478=
ENST00000544905.1:c.160G=
ENST00000595085.5:c.922+1903G= ENSP00000471150.2:n.922+1903G=
NM_000709.3:c.1330G= NP_000700.1:p.Asp444=
NM_001164783.1:c.1327G= NP_001158255.1:p.Asp443=
NM_000709.4:c.1330G= MANE Select NP_000700.1:p.Asp444=
NM_001164783.2:c.1327G= NP_001158255.1:p.Asp443=