Canonical Allele Identifier: CA2336459961
Gene: BCKDHA HGNC NCBI

Linked Data

dbSNP Id: rs2039403317

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41424318A>T , CM000681.2:g.41424318A>T GRCh38
NC_000019.9:g.41930223A>T , CM000681.1:g.41930223A>T GRCh37
NC_000019.8:g.46622063A>T NCBI36
NG_013004.1:g.31530A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.1168-120A>T MANE Select ENSP00000269980.2:n.1168-120A>T
ENST00000269980.6:c.1168-120A>T ENSP00000269980.2:n.1168-120A>T
ENST00000457836.6:c.1177-120A>T ENSP00000416000.2:n.1177-120A>T
ENST00000540732.3:c.1270-120A>T ENSP00000443246.1:n.1270-120A>T
ENST00000544905.1:c.62-184A>T
ENST00000595085.5:c.922+1621A>T ENSP00000471150.2:n.922+1621A>T
NM_000709.3:c.1168-120A>T NP_000700.1:n.1168-120A>T
NM_001164783.1:c.1165-120A>T NP_001158255.1:n.1165-120A>T
NM_000709.4:c.1168-120A>T MANE Select NP_000700.1:n.1168-120A>T
NM_001164783.2:c.1165-120A>T NP_001158255.1:n.1165-120A>T