Canonical Allele Identifier: CA406015290

Gene: BCKDHA

Linked Data

• MyVariant Identifiers: chr19:g.41930376C>T (hg19) ; chr19:g.41424471C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41424471C>T , CM000681.2:g.41424471C>T	GRCh38
NC_000019.9:g.41930376C>T , CM000681.1:g.41930376C>T	GRCh37
NC_000019.8:g.46622216C>T	NCBI36
NG_013004.1:g.31683C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269980.7:c.1201C>T MANE Select	ENSP00000269980.2:p.Pro401Ser
ENST00000269980.6:c.1201C>T	ENSP00000269980.2:p.Pro401Ser
ENST00000457836.6:c.1210C>T	ENSP00000416000.2:p.Pro404Ser
ENST00000540732.3:c.1303C>T	ENSP00000443246.1:p.Pro435Ser
ENST00000544905.1:c.62-31C>T
ENST00000595085.5:c.922+1774C>T	ENSP00000471150.2:n.922+1774C>T
NM_000709.3:c.1201C>T	NP_000700.1:p.Pro401Ser
NM_001164783.1:c.1198C>T	NP_001158255.1:p.Pro400Ser
NM_000709.4:c.1201C>T MANE Select	NP_000700.1:p.Pro401Ser
NM_001164783.2:c.1198C>T	NP_001158255.1:p.Pro400Ser