Canonical Allele Identifier: CA1941711186
Gene: ACADSB HGNC NCBI

Linked Data

dbSNP Id: rs1850366019

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.123034263dup , CM000672.2:g.123034263dup GRCh38
NC_000010.10:g.124793779dup , CM000672.1:g.124793779dup GRCh37
NC_000010.9:g.124783769dup NCBI36
NG_008003.1:g.30351dup , LRG_451:g.30351dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000358776.7:c.43-93dup MANE Select ENSP00000357873.3:n.43-93dup
ENST00000358776.6:c.43-93dup ENSP00000357873.3:n.43-93dup
ENST00000368869.8:c.-163-93dup ENSP00000357862.4:n.-163-93dup
ENST00000411816.2:n.60-93dup
NM_001609.3:c.43-93dup , LRG_451t1:c.43-93dup NP_001600.1:n.43-93dup
NM_001330174.1:c.-163-93dup NP_001317103.1:n.-163-93dup
NM_001330174.2:c.-163-93dup NP_001317103.1:n.-163-93dup
NM_001609.4:c.43-93dup MANE Select NP_001600.1:n.43-93dup
NM_001330174.3:c.-163-93dup NP_001317103.1:n.-163-93dup