Canonical Allele Identifier: CA406013714
Gene: BCKDHA HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.41928896T>A (hg19) chr19:g.41422991T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41422991T>A , CM000681.2:g.41422991T>A GRCh38
NC_000019.9:g.41928896T>A , CM000681.1:g.41928896T>A GRCh37
NC_000019.8:g.46620736T>A NCBI36
NG_013004.1:g.30203T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.996-7T>A MANE Select ENSP00000269980.2:n.996-7T>A
ENST00000269980.6:c.996-7T>A ENSP00000269980.2:n.996-7T>A
ENST00000457836.6:c.998T>A ENSP00000416000.2:p.Leu333Gln
ENST00000540732.3:c.1098-7T>A ENSP00000443246.1:n.1098-7T>A
ENST00000542943.5:c.909-7T>A ENSP00000440345.1:n.909-7T>A
ENST00000595085.5:c.922+294T>A ENSP00000471150.2:n.922+294T>A
NM_000709.3:c.996-7T>A NP_000700.1:n.996-7T>A
NM_001164783.1:c.993-7T>A NP_001158255.1:n.993-7T>A
NM_000709.4:c.996-7T>A MANE Select NP_000700.1:n.996-7T>A
NM_001164783.2:c.993-7T>A NP_001158255.1:n.993-7T>A
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