Canonical Allele Identifier: CA2336455319
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41414059C= , CM000681.2:g.41414059C= GRCh38
NC_000019.9:g.41919964C= , CM000681.1:g.41919964C= GRCh37
NC_000019.8:g.46611804C= NCBI36
NG_013004.1:g.21271C=

Transcript Alleles

HGVS Amino-acid change
ENST00000269980.7:c.386C= MANE Select ENSP00000269980.2:p.Ser129=
ENST00000269980.6:c.386C= ENSP00000269980.2:p.Ser129=
ENST00000457836.6:c.320C= ENSP00000416000.2:p.Ser107=
ENST00000538423.5:n.512C=
ENST00000540732.3:c.488C= ENSP00000443246.1:p.Ser163=
ENST00000541315.1:c.193C=
ENST00000542943.5:c.299C= ENSP00000440345.1:p.Ser100=
ENST00000595085.5:c.386C= ENSP00000471150.2:p.Ser129=
NM_000709.3:c.386C= NP_000700.1:p.Ser129=
NM_001164783.1:c.386C= NP_001158255.1:p.Ser129=
NM_000709.4:c.386C= MANE Select NP_000700.1:p.Ser129=
NM_001164783.2:c.386C= NP_001158255.1:p.Ser129=