Canonical Allele Identifier: CA2336459399
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41423016C= , CM000681.2:g.41423016C= GRCh38
NC_000019.9:g.41928921C= , CM000681.1:g.41928921C= GRCh37
NC_000019.8:g.46620761C= NCBI36
NG_013004.1:g.30228C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.1014C= MANE Select ENSP00000269980.2:p.Thr338=
ENST00000269980.6:c.1014C= ENSP00000269980.2:p.Thr338=
ENST00000457836.6:c.1023C= ENSP00000416000.2:p.Thr341=
ENST00000540732.3:c.1116C= ENSP00000443246.1:p.Thr372=
ENST00000542943.5:c.927C= ENSP00000440345.1:p.Thr309=
ENST00000595085.5:c.922+319C= ENSP00000471150.2:n.922+319C=
NM_000709.3:c.1014C= NP_000700.1:p.Thr338=
NM_001164783.1:c.1011C= NP_001158255.1:p.Thr337=
NM_000709.4:c.1014C= MANE Select NP_000700.1:p.Thr338=
NM_001164783.2:c.1011C= NP_001158255.1:p.Thr337=