Canonical Allele Identifier: CA507555389

Gene: BCKDHA

Linked Data

• MyVariant Identifiers: chr19:g.41916574T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41410669T>C , CM000681.2:g.41410669T>C	GRCh38
NC_000019.9:g.41916574T>C , CM000681.1:g.41916574T>C	GRCh37
NC_000019.8:g.46608414T>C	NCBI36
NG_013004.1:g.17881T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000269980.7:c.141T>C MANE Select	ENSP00000269980.2:p.Ser47=
ENST00000269980.6:c.141T>C	ENSP00000269980.2:p.Ser47=
ENST00000457836.6:c.75T>C	ENSP00000416000.2:p.Ser25=
ENST00000538423.5:n.161T>C
ENST00000540732.3:c.243T>C	ENSP00000443246.1:p.Ser81=
ENST00000542943.5:c.141T>C	ENSP00000440345.1:p.Ser47=
ENST00000595085.5:c.141T>C	ENSP00000471150.2:p.Ser47=
ENST00000604424.1:n.383T>C
NM_000709.3:c.141T>C	NP_000700.1:p.Ser47=
NM_001164783.1:c.141T>C	NP_001158255.1:p.Ser47=
NM_000709.4:c.141T>C MANE Select	NP_000700.1:p.Ser47=
NM_001164783.2:c.141T>C	NP_001158255.1:p.Ser47=