Canonical Allele Identifier: CA6831134
Gene: ACADS HGNC NCBI

Linked Data

dbSNP Id: rs766506561
ExAC: 12:121176580 A / AG
gnomAD v2: 12-121176580-A-AG
gnomAD v3: 12-120738777-A-AG
gnomAD v4: 12-120738777-A-AG
MyVariant Identifiers: chr12:g.121176580_121176581insG (hg19) chr12:g.120738777_120738778insG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120738781dup , CM000674.2:g.120738781dup GRCh38
NC_000012.11:g.121176584dup , CM000674.1:g.121176584dup GRCh37
NC_000012.10:g.119660967dup NCBI36
NG_007991.1:g.18014dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.934-39dup MANE Select ENSP00000242592.4:n.934-39dup
ENST00000242592.8:c.934-39dup ENSP00000242592.4:n.934-39dup
ENST00000411593.2:c.922-39dup ENSP00000401045.2:n.922-39dup
NM_000017.3:c.934-39dup NP_000008.1:n.934-39dup
NM_001302554.1:c.922-39dup NP_001289483.1:n.922-39dup
NM_000017.4:c.934-39dup MANE Select NP_000008.1:n.934-39dup
NM_001302554.2:c.922-39dup NP_001289483.1:n.922-39dup
Search 100 bp 5'
Search 100 bp 3'