Canonical Allele Identifier: CA2585308344
Gene: BCKDHA HGNC NCBI

Linked Data

gnomAD v4: 19-41424287-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41424287T>C , CM000681.2:g.41424287T>C GRCh38
NC_000019.9:g.41930192T>C , CM000681.1:g.41930192T>C GRCh37
NC_000019.8:g.46622032T>C NCBI36
NG_013004.1:g.31499T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.1168-151T>C MANE Select ENSP00000269980.2:n.1168-151T>C
ENST00000269980.6:c.1168-151T>C ENSP00000269980.2:n.1168-151T>C
ENST00000457836.6:c.1177-151T>C ENSP00000416000.2:n.1177-151T>C
ENST00000540732.3:c.1270-151T>C ENSP00000443246.1:n.1270-151T>C
ENST00000544905.1:c.62-215T>C
ENST00000595085.5:c.922+1590T>C ENSP00000471150.2:n.922+1590T>C
NM_000709.3:c.1168-151T>C NP_000700.1:n.1168-151T>C
NM_001164783.1:c.1165-151T>C NP_001158255.1:n.1165-151T>C
NM_000709.4:c.1168-151T>C MANE Select NP_000700.1:n.1168-151T>C
NM_001164783.2:c.1165-151T>C NP_001158255.1:n.1165-151T>C
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