Canonical Allele Identifier: CA2336458873
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41421950A= , CM000681.2:g.41421950A= GRCh38
NC_000019.9:g.41927855A= , CM000681.1:g.41927855A= GRCh37
NC_000019.8:g.46619695A= NCBI36
NG_013004.1:g.29162A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.647-214A= MANE Select ENSP00000269980.2:n.647-214A=
ENST00000269980.6:c.647-214A= ENSP00000269980.2:n.647-214A=
ENST00000457836.6:c.581-214A= ENSP00000416000.2:n.581-214A=
ENST00000535632.5:n.276-214A=
ENST00000538423.5:n.773-214A=
ENST00000540732.3:c.749-214A= ENSP00000443246.1:n.749-214A=
ENST00000541315.1:c.547-214A=
ENST00000542943.5:c.560-214A= ENSP00000440345.1:n.560-214A=
ENST00000545787.1:n.275-214A=
ENST00000595085.5:c.647-214A= ENSP00000471150.2:n.647-214A=
NM_000709.3:c.647-214A= NP_000700.1:n.647-214A=
NM_001164783.1:c.647-214A= NP_001158255.1:n.647-214A=
NM_000709.4:c.647-214A= MANE Select NP_000700.1:n.647-214A=
NM_001164783.2:c.647-214A= NP_001158255.1:n.647-214A=