Canonical Allele Identifier: CA2585308194

Gene: BCKDHA

Linked Data

• gnomAD v4: 19-41422913-CCTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41422915_41422917del , CM000681.2:g.41422915_41422917del	GRCh38
NC_000019.9:g.41928820_41928822del , CM000681.1:g.41928820_41928822del	GRCh37
NC_000019.8:g.46620660_46620662del	NCBI36
NG_013004.1:g.30127_30129del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269980.7:c.996-83_996-81del MANE Select	ENSP00000269980.2:n.996-83_996-81del
ENST00000269980.6:c.996-83_996-81del	ENSP00000269980.2:n.996-83_996-81del
ENST00000457836.6:c.930-8_930-6del	ENSP00000416000.2:n.930-8_930-6del
ENST00000540732.3:c.1098-83_1098-81del	ENSP00000443246.1:n.1098-83_1098-81del
ENST00000542943.5:c.909-83_909-81del	ENSP00000440345.1:n.909-83_909-81del
ENST00000595085.5:c.922+218_922+220del	ENSP00000471150.2:n.922+218_922+220del
NM_000709.3:c.996-83_996-81del	NP_000700.1:n.996-83_996-81del
NM_001164783.1:c.993-83_993-81del	NP_001158255.1:n.993-83_993-81del
NM_000709.4:c.996-83_996-81del MANE Select	NP_000700.1:n.996-83_996-81del
NM_001164783.2:c.993-83_993-81del	NP_001158255.1:n.993-83_993-81del