Canonical Allele Identifier: CA406012666

Gene: BCKDHA

Linked Data

• gnomAD v4: 19-41422167-T-G
• MyVariant Identifiers: chr19:g.41928072T>G (hg19) ; chr19:g.41422167T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41422167T>G , CM000681.2:g.41422167T>G	GRCh38
NC_000019.9:g.41928072T>G , CM000681.1:g.41928072T>G	GRCh37
NC_000019.8:g.46619912T>G	NCBI36
NG_013004.1:g.29379T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000269980.7:c.650T>G MANE Select	ENSP00000269980.2:p.Val217Gly
ENST00000269980.6:c.650T>G	ENSP00000269980.2:p.Val217Gly
ENST00000457836.6:c.584T>G	ENSP00000416000.2:p.Val195Gly
ENST00000535632.5:n.279T>G
ENST00000538423.5:n.776T>G
ENST00000540732.3:c.752T>G	ENSP00000443246.1:p.Val251Gly
ENST00000541315.1:c.550T>G
ENST00000542943.5:c.563T>G	ENSP00000440345.1:p.Val188Gly
ENST00000545787.1:n.278T>G
ENST00000595085.5:c.650T>G	ENSP00000471150.2:p.Val217Gly
NM_000709.3:c.650T>G	NP_000700.1:p.Val217Gly
NM_001164783.1:c.650T>G	NP_001158255.1:p.Val217Gly
NM_000709.4:c.650T>G MANE Select	NP_000700.1:p.Val217Gly
NM_001164783.2:c.650T>G	NP_001158255.1:p.Val217Gly