Canonical Allele Identifier: CA406015510

Gene: BCKDHA

Linked Data

• dbSNP Id: rs141991700
• MyVariant Identifiers: chr19:g.41930445C>T (hg19) ; chr19:g.41424540C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41424540C>T , CM000681.2:g.41424540C>T	GRCh38
NC_000019.9:g.41930445C>T , CM000681.1:g.41930445C>T	GRCh37
NC_000019.8:g.46622285C>T	NCBI36
NG_013004.1:g.31752C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269980.7:c.1270C>T MANE Select	ENSP00000269980.2:p.Gln424Ter
ENST00000269980.6:c.1270C>T	ENSP00000269980.2:p.Gln424Ter
ENST00000457836.6:c.1279C>T	ENSP00000416000.2:p.Gln427Ter
ENST00000540732.3:c.1372C>T	ENSP00000443246.1:p.Gln458Ter
ENST00000544905.1:c.100C>T
ENST00000595085.5:c.922+1843C>T	ENSP00000471150.2:n.922+1843C>T
NM_000709.3:c.1270C>T	NP_000700.1:p.Gln424Ter
NM_001164783.1:c.1267C>T	NP_001158255.1:p.Gln423Ter
NM_000709.4:c.1270C>T MANE Select	NP_000700.1:p.Gln424Ter
NM_001164783.2:c.1267C>T	NP_001158255.1:p.Gln423Ter