Canonical Allele Identifier: CA2585306888

Gene: BCKDHA

Linked Data

• gnomAD v4: 19-41411106-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41411112dup , CM000681.2:g.41411112dup	GRCh38
NC_000019.9:g.41917017dup , CM000681.1:g.41917017dup	GRCh37
NC_000019.8:g.46608857dup	NCBI36
NG_013004.1:g.18324dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269980.7:c.375+103dup MANE Select	ENSP00000269980.2:n.375+103dup
ENST00000269980.6:c.375+103dup	ENSP00000269980.2:n.375+103dup
ENST00000457836.6:c.309+103dup	ENSP00000416000.2:n.309+103dup
ENST00000538423.5:n.501+103dup
ENST00000540732.3:c.477+103dup	ENSP00000443246.1:n.477+103dup
ENST00000541315.1:c.182+103dup
ENST00000542943.5:c.288+296dup	ENSP00000440345.1:n.288+296dup
ENST00000595085.5:c.375+103dup	ENSP00000471150.2:n.375+103dup
NM_000709.3:c.375+103dup	NP_000700.1:n.375+103dup
NM_001164783.1:c.375+103dup	NP_001158255.1:n.375+103dup
NM_000709.4:c.375+103dup MANE Select	NP_000700.1:n.375+103dup
NM_001164783.2:c.375+103dup	NP_001158255.1:n.375+103dup