Canonical Allele Identifier: CA2336453983
Gene: BCKDHA HGNC NCBI

Linked Data

dbSNP Id: rs748582297

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41411039G>A , CM000681.2:g.41411039G>A GRCh38
NC_000019.9:g.41916944G>A , CM000681.1:g.41916944G>A GRCh37
NC_000019.8:g.46608784G>A NCBI36
NG_013004.1:g.18251G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.375+30G>A MANE Select ENSP00000269980.2:n.375+30G>A
ENST00000269980.6:c.375+30G>A ENSP00000269980.2:n.375+30G>A
ENST00000457836.6:c.309+30G>A ENSP00000416000.2:n.309+30G>A
ENST00000538423.5:n.501+30G>A
ENST00000540732.3:c.477+30G>A ENSP00000443246.1:n.477+30G>A
ENST00000541315.1:c.182+30G>A
ENST00000542943.5:c.288+223G>A ENSP00000440345.1:n.288+223G>A
ENST00000595085.5:c.375+30G>A ENSP00000471150.2:n.375+30G>A
NM_000709.3:c.375+30G>A NP_000700.1:n.375+30G>A
NM_001164783.1:c.375+30G>A NP_001158255.1:n.375+30G>A
NM_000709.4:c.375+30G>A MANE Select NP_000700.1:n.375+30G>A
NM_001164783.2:c.375+30G>A NP_001158255.1:n.375+30G>A