Canonical Allele Identifier: CA308527671

Gene: BCKDHA

Linked Data

• dbSNP Id: rs1018367222
• gnomAD v2: 19-41930229-G-A
• gnomAD v3: 19-41424324-G-A
• gnomAD v4: 19-41424324-G-A
• MyVariant Identifiers: chr19:g.41930229G>A (hg19) ; chr19:g.41424324G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41424324G>A , CM000681.2:g.41424324G>A	GRCh38
NC_000019.9:g.41930229G>A , CM000681.1:g.41930229G>A	GRCh37
NC_000019.8:g.46622069G>A	NCBI36
NG_013004.1:g.31536G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269980.7:c.1168-114G>A MANE Select	ENSP00000269980.2:n.1168-114G>A
ENST00000269980.6:c.1168-114G>A	ENSP00000269980.2:n.1168-114G>A
ENST00000457836.6:c.1177-114G>A	ENSP00000416000.2:n.1177-114G>A
ENST00000540732.3:c.1270-114G>A	ENSP00000443246.1:n.1270-114G>A
ENST00000544905.1:c.62-178G>A
ENST00000595085.5:c.922+1627G>A	ENSP00000471150.2:n.922+1627G>A
NM_000709.3:c.1168-114G>A	NP_000700.1:n.1168-114G>A
NM_001164783.1:c.1165-114G>A	NP_001158255.1:n.1165-114G>A
NM_000709.4:c.1168-114G>A MANE Select	NP_000700.1:n.1168-114G>A
NM_001164783.2:c.1165-114G>A	NP_001158255.1:n.1165-114G>A