Canonical Allele Identifier: CA406013270

Gene: BCKDHA

Linked Data

• MyVariant Identifiers: chr19:g.41928554G>A (hg19) ; chr19:g.41422649G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41422649G>A , CM000681.2:g.41422649G>A	GRCh38
NC_000019.9:g.41928554G>A , CM000681.1:g.41928554G>A	GRCh37
NC_000019.8:g.46620394G>A	NCBI36
NG_013004.1:g.29861G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000269980.7:c.874G>A MANE Select	ENSP00000269980.2:p.Gly292Ser
ENST00000269980.6:c.874G>A	ENSP00000269980.2:p.Gly292Ser
ENST00000457836.6:c.808G>A	ENSP00000416000.2:p.Gly270Ser
ENST00000535632.5:n.503G>A
ENST00000540732.3:c.976G>A	ENSP00000443246.1:p.Gly326Ser
ENST00000542943.5:c.787G>A	ENSP00000440345.1:p.Gly263Ser
ENST00000545787.1:n.502G>A
ENST00000595085.5:c.874G>A	ENSP00000471150.2:p.Gly292Ser
NM_000709.3:c.874G>A	NP_000700.1:p.Gly292Ser
NM_001164783.1:c.871G>A	NP_001158255.1:p.Gly291Ser
NM_000709.4:c.874G>A MANE Select	NP_000700.1:p.Gly292Ser
NM_001164783.2:c.871G>A	NP_001158255.1:p.Gly291Ser