Canonical Allele Identifier: CA2789793009
Gene: ACADSB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.123034552G>C , CM000672.2:g.123034552G>C GRCh38
NC_000010.10:g.124794068G>C , CM000672.1:g.124794068G>C GRCh37
NC_000010.9:g.124784058G>C NCBI36
NG_008003.1:g.30640G>C , LRG_451:g.30640G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000358776.7:c.202+37G>C MANE Select ENSP00000357873.3:n.202+37G>C
ENST00000358776.6:c.202+37G>C ENSP00000357873.3:n.202+37G>C
ENST00000368869.8:c.-4+37G>C ENSP00000357862.4:n.-4+37G>C
ENST00000411816.2:n.219+37G>C
NM_001609.3:c.202+37G>C , LRG_451t1:c.202+37G>C NP_001600.1:n.202+37G>C
NM_001330174.1:c.-4+37G>C NP_001317103.1:n.-4+37G>C
NM_001330174.2:c.-4+37G>C NP_001317103.1:n.-4+37G>C
NM_001609.4:c.202+37G>C MANE Select NP_001600.1:n.202+37G>C
NM_001330174.3:c.-4+37G>C NP_001317103.1:n.-4+37G>C