Canonical Allele Identifier: CA406015317

Gene: BCKDHA

Linked Data

• MyVariant Identifiers: chr19:g.41930382C>T (hg19) ; chr19:g.41424477C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41424477C>T , CM000681.2:g.41424477C>T	GRCh38
NC_000019.9:g.41930382C>T , CM000681.1:g.41930382C>T	GRCh37
NC_000019.8:g.46622222C>T	NCBI36
NG_013004.1:g.31689C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269980.7:c.1207C>T MANE Select	ENSP00000269980.2:p.Pro403Ser
ENST00000269980.6:c.1207C>T	ENSP00000269980.2:p.Pro403Ser
ENST00000457836.6:c.1216C>T	ENSP00000416000.2:p.Pro406Ser
ENST00000540732.3:c.1309C>T	ENSP00000443246.1:p.Pro437Ser
ENST00000544905.1:c.62-25C>T
ENST00000595085.5:c.922+1780C>T	ENSP00000471150.2:n.922+1780C>T
NM_000709.3:c.1207C>T	NP_000700.1:p.Pro403Ser
NM_001164783.1:c.1204C>T	NP_001158255.1:p.Pro402Ser
NM_000709.4:c.1207C>T MANE Select	NP_000700.1:p.Pro403Ser
NM_001164783.2:c.1204C>T	NP_001158255.1:p.Pro402Ser