Canonical Allele Identifier: CA406007814
Community Standard Title: NM_000709.4(BCKDHA):c.405T>G (p.Tyr135Ter)
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41414078T>G , CM000681.2:g.41414078T>G GRCh38
NC_000019.9:g.41919983T>G , CM000681.1:g.41919983T>G GRCh37
NC_000019.8:g.46611823T>G NCBI36
NG_013004.1:g.21290T>G

Transcript Alleles

HGVS Amino-acid Change
NM_000709.4:c.405T>G MANE Select NP_000700.1:p.Tyr135Ter
ENST00000269980.7:c.405T>G MANE Select ENSP00000269980.2:p.Tyr135Ter
NM_000709.3:c.405T>G NP_000700.1:p.Tyr135Ter
NM_001164783.1:c.405T>G NP_001158255.1:p.Tyr135Ter
NM_001164783.2:c.405T>G NP_001158255.1:p.Tyr135Ter
ENST00000269980.6:c.405T>G ENSP00000269980.2:p.Tyr135Ter
ENST00000457836.6:c.339T>G ENSP00000416000.2:p.Tyr113Ter
ENST00000538423.5:n.531T>G
ENST00000540732.3:c.507T>G ENSP00000443246.1:p.Tyr169Ter
ENST00000541315.1:c.212T>G
ENST00000542943.5:c.318T>G ENSP00000440345.1:p.Tyr106Ter
ENST00000595085.5:c.405T>G ENSP00000471150.2:p.Tyr135Ter