Canonical Allele Identifier: CA406015382

Gene: BCKDHA

Linked Data

• MyVariant Identifiers: chr19:g.41930407A>C (hg19) ; chr19:g.41424502A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41424502A>C , CM000681.2:g.41424502A>C	GRCh38
NC_000019.9:g.41930407A>C , CM000681.1:g.41930407A>C	GRCh37
NC_000019.8:g.46622247A>C	NCBI36
NG_013004.1:g.31714A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269980.7:c.1232A>C MANE Select	ENSP00000269980.2:p.Asp411Ala
ENST00000269980.6:c.1232A>C	ENSP00000269980.2:p.Asp411Ala
ENST00000457836.6:c.1241A>C	ENSP00000416000.2:p.Asp414Ala
ENST00000540732.3:c.1334A>C	ENSP00000443246.1:p.Asp445Ala
ENST00000544905.1:c.62A>C
ENST00000595085.5:c.922+1805A>C	ENSP00000471150.2:n.922+1805A>C
NM_000709.3:c.1232A>C	NP_000700.1:p.Asp411Ala
NM_001164783.1:c.1229A>C	NP_001158255.1:p.Asp410Ala
NM_000709.4:c.1232A>C MANE Select	NP_000700.1:p.Asp411Ala
NM_001164783.2:c.1229A>C	NP_001158255.1:p.Asp410Ala