Canonical Allele Identifier: CA406012770
Gene: BCKDHA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41422221A>T , CM000681.2:g.41422221A>T GRCh38
NC_000019.9:g.41928126A>T , CM000681.1:g.41928126A>T GRCh37
NC_000019.8:g.46619966A>T NCBI36
NG_013004.1:g.29433A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.704A>T MANE Select ENSP00000269980.2:p.Tyr235Phe
ENST00000269980.6:c.704A>T ENSP00000269980.2:p.Tyr235Phe
ENST00000457836.6:c.638A>T ENSP00000416000.2:p.Tyr213Phe
ENST00000535632.5:n.333A>T
ENST00000540732.3:c.806A>T ENSP00000443246.1:p.Tyr269Phe
ENST00000541315.1:c.604A>T
ENST00000542943.5:c.617A>T ENSP00000440345.1:p.Tyr206Phe
ENST00000545787.1:n.332A>T
ENST00000595085.5:c.704A>T ENSP00000471150.2:p.Tyr235Phe
NM_000709.3:c.704A>T NP_000700.1:p.Tyr235Phe
NM_001164783.1:c.704A>T NP_001158255.1:p.Tyr235Phe
NM_000709.4:c.704A>T MANE Select NP_000700.1:p.Tyr235Phe
NM_001164783.2:c.704A>T NP_001158255.1:p.Tyr235Phe