Canonical Allele Identifier: CA633470476
Gene: BCKDHA HGNC NCBI

Linked Data

dbSNP Id: rs1347404337

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41424415C>T , CM000681.2:g.41424415C>T GRCh38
NC_000019.9:g.41930320C>T , CM000681.1:g.41930320C>T GRCh37
NC_000019.8:g.46622160C>T NCBI36
NG_013004.1:g.31627C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000269980.7:c.1168-23C>T MANE Select ENSP00000269980.2:n.1168-23C>T
ENST00000269980.6:c.1168-23C>T ENSP00000269980.2:n.1168-23C>T
ENST00000457836.6:c.1177-23C>T ENSP00000416000.2:n.1177-23C>T
ENST00000540732.3:c.1270-23C>T ENSP00000443246.1:n.1270-23C>T
ENST00000544905.1:c.62-87C>T
ENST00000595085.5:c.922+1718C>T ENSP00000471150.2:n.922+1718C>T
NM_000709.3:c.1168-23C>T NP_000700.1:n.1168-23C>T
NM_001164783.1:c.1165-23C>T NP_001158255.1:n.1165-23C>T
NM_000709.4:c.1168-23C>T MANE Select NP_000700.1:n.1168-23C>T
NM_001164783.2:c.1165-23C>T NP_001158255.1:n.1165-23C>T