Canonical Allele Identifier: CA2336458871

Gene: BCKDHA

Linked Data

• dbSNP Id: rs2039370401

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41421947_41421981del , CM000681.2:g.41421947_41421981del	GRCh38
NC_000019.9:g.41927852_41927886del , CM000681.1:g.41927852_41927886del	GRCh37
NC_000019.8:g.46619692_46619726del	NCBI36
NG_013004.1:g.29159_29193del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269980.7:c.647-217_647-183del MANE Select	ENSP00000269980.2:n.647-217_647-183del
ENST00000269980.6:c.647-217_647-183del	ENSP00000269980.2:n.647-217_647-183del
ENST00000457836.6:c.581-217_581-183del	ENSP00000416000.2:n.581-217_581-183del
ENST00000535632.5:n.276-217_276-183del
ENST00000538423.5:n.773-217_773-183del
ENST00000540732.3:c.749-217_749-183del	ENSP00000443246.1:n.749-217_749-183del
ENST00000541315.1:c.547-217_547-183del
ENST00000542943.5:c.560-217_560-183del	ENSP00000440345.1:n.560-217_560-183del
ENST00000545787.1:n.275-217_275-183del
ENST00000595085.5:c.647-217_647-183del	ENSP00000471150.2:n.647-217_647-183del
NM_000709.3:c.647-217_647-183del	NP_000700.1:n.647-217_647-183del
NM_001164783.1:c.647-217_647-183del	NP_001158255.1:n.647-217_647-183del
NM_000709.4:c.647-217_647-183del MANE Select	NP_000700.1:n.647-217_647-183del
NM_001164783.2:c.647-217_647-183del	NP_001158255.1:n.647-217_647-183del