Canonical Allele Identifier: CA406013774

Gene: BCKDHA

Linked Data

• MyVariant Identifiers: chr19:g.41928919A>T (hg19) ; chr19:g.41423014A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41423014A>T , CM000681.2:g.41423014A>T	GRCh38
NC_000019.9:g.41928919A>T , CM000681.1:g.41928919A>T	GRCh37
NC_000019.8:g.46620759A>T	NCBI36
NG_013004.1:g.30226A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269980.7:c.1012A>T MANE Select	ENSP00000269980.2:p.Thr338Ser
ENST00000269980.6:c.1012A>T	ENSP00000269980.2:p.Thr338Ser
ENST00000457836.6:c.1021A>T	ENSP00000416000.2:p.Thr341Ser
ENST00000540732.3:c.1114A>T	ENSP00000443246.1:p.Thr372Ser
ENST00000542943.5:c.925A>T	ENSP00000440345.1:p.Thr309Ser
ENST00000595085.5:c.922+317A>T	ENSP00000471150.2:n.922+317A>T
NM_000709.3:c.1012A>T	NP_000700.1:p.Thr338Ser
NM_001164783.1:c.1009A>T	NP_001158255.1:p.Thr337Ser
NM_000709.4:c.1012A>T MANE Select	NP_000700.1:p.Thr338Ser
NM_001164783.2:c.1009A>T	NP_001158255.1:p.Thr337Ser