Canonical Allele Identifier: CA9461392

Gene: BCKDHA

Linked Data

• dbSNP Id: rs780357653
• ExAC: 19:41930330 C / G
• gnomAD v2: 19-41930330-C-G
• gnomAD v4: 19-41424425-C-G
• MyVariant Identifiers: chr19:g.41930330C>G (hg19) ; chr19:g.41424425C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41424425C>G , CM000681.2:g.41424425C>G	GRCh38
NC_000019.9:g.41930330C>G , CM000681.1:g.41930330C>G	GRCh37
NC_000019.8:g.46622170C>G	NCBI36
NG_013004.1:g.31637C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000269980.7:c.1168-13C>G MANE Select	ENSP00000269980.2:n.1168-13C>G
ENST00000269980.6:c.1168-13C>G	ENSP00000269980.2:n.1168-13C>G
ENST00000457836.6:c.1177-13C>G	ENSP00000416000.2:n.1177-13C>G
ENST00000540732.3:c.1270-13C>G	ENSP00000443246.1:n.1270-13C>G
ENST00000544905.1:c.62-77C>G
ENST00000595085.5:c.922+1728C>G	ENSP00000471150.2:n.922+1728C>G
NM_000709.3:c.1168-13C>G	NP_000700.1:n.1168-13C>G
NM_001164783.1:c.1165-13C>G	NP_001158255.1:n.1165-13C>G
NM_000709.4:c.1168-13C>G MANE Select	NP_000700.1:n.1168-13C>G
NM_001164783.2:c.1165-13C>G	NP_001158255.1:n.1165-13C>G