Canonical Allele Identifier: CA406012765
Gene: BCKDHA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41422220T>A , CM000681.2:g.41422220T>A GRCh38
NC_000019.9:g.41928125T>A , CM000681.1:g.41928125T>A GRCh37
NC_000019.8:g.46619965T>A NCBI36
NG_013004.1:g.29432T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.703T>A MANE Select ENSP00000269980.2:p.Tyr235Asn
ENST00000269980.6:c.703T>A ENSP00000269980.2:p.Tyr235Asn
ENST00000457836.6:c.637T>A ENSP00000416000.2:p.Tyr213Asn
ENST00000535632.5:n.332T>A
ENST00000540732.3:c.805T>A ENSP00000443246.1:p.Tyr269Asn
ENST00000541315.1:c.603T>A
ENST00000542943.5:c.616T>A ENSP00000440345.1:p.Tyr206Asn
ENST00000545787.1:n.331T>A
ENST00000595085.5:c.703T>A ENSP00000471150.2:p.Tyr235Asn
NM_000709.3:c.703T>A NP_000700.1:p.Tyr235Asn
NM_001164783.1:c.703T>A NP_001158255.1:p.Tyr235Asn
NM_000709.4:c.703T>A MANE Select NP_000700.1:p.Tyr235Asn
NM_001164783.2:c.703T>A NP_001158255.1:p.Tyr235Asn