Canonical Allele Identifier: CA2336460016
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41424433C= , CM000681.2:g.41424433C= GRCh38
NC_000019.9:g.41930338C= , CM000681.1:g.41930338C= GRCh37
NC_000019.8:g.46622178C= NCBI36
NG_013004.1:g.31645C=

Transcript Alleles

HGVS Amino-acid change
ENST00000269980.7:c.1168-5C= MANE Select ENSP00000269980.2:n.1168-5C=
ENST00000269980.6:c.1168-5C= ENSP00000269980.2:n.1168-5C=
ENST00000457836.6:c.1177-5C= ENSP00000416000.2:n.1177-5C=
ENST00000540732.3:c.1270-5C= ENSP00000443246.1:n.1270-5C=
ENST00000544905.1:c.62-69C=
ENST00000595085.5:c.922+1736C= ENSP00000471150.2:n.922+1736C=
NM_000709.3:c.1168-5C= NP_000700.1:n.1168-5C=
NM_001164783.1:c.1165-5C= NP_001158255.1:n.1165-5C=
NM_000709.4:c.1168-5C= MANE Select NP_000700.1:n.1168-5C=
NM_001164783.2:c.1165-5C= NP_001158255.1:n.1165-5C=