Canonical Allele Identifier: CA507560647
Gene: BCKDHA HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.41930293G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41424388G>A , CM000681.2:g.41424388G>A GRCh38
NC_000019.9:g.41930293G>A , CM000681.1:g.41930293G>A GRCh37
NC_000019.8:g.46622133G>A NCBI36
NG_013004.1:g.31600G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000269980.7:c.1168-50G>A MANE Select ENSP00000269980.2:n.1168-50G>A
ENST00000269980.6:c.1168-50G>A ENSP00000269980.2:n.1168-50G>A
ENST00000457836.6:c.1177-50G>A ENSP00000416000.2:n.1177-50G>A
ENST00000540732.3:c.1270-50G>A ENSP00000443246.1:n.1270-50G>A
ENST00000544905.1:c.62-114G>A
ENST00000595085.5:c.922+1691G>A ENSP00000471150.2:n.922+1691G>A
NM_000709.3:c.1168-50G>A NP_000700.1:n.1168-50G>A
NM_001164783.1:c.1165-50G>A NP_001158255.1:n.1165-50G>A
NM_000709.4:c.1168-50G>A MANE Select NP_000700.1:n.1168-50G>A
NM_001164783.2:c.1165-50G>A NP_001158255.1:n.1165-50G>A
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