Canonical Allele Identifier: CA6831195
Gene: ACADS HGNC NCBI

Linked Data

ClinVar Variation Id: 716376
ClinVar RCV Id: RCV002540082
dbSNP Id: rs145594828
ExAC: 12:121176966 C / T
gnomAD v2: 12-121176966-C-T
gnomAD v3: 12-120739163-C-T
gnomAD v4: 12-120739163-C-T
MyVariant Identifiers: chr12:g.121176966C>T (hg19) chr12:g.120739163C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120739163C>T , CM000674.2:g.120739163C>T GRCh38
NC_000012.11:g.121176966C>T , CM000674.1:g.121176966C>T GRCh37
NC_000012.10:g.119661349C>T NCBI36
NG_007991.1:g.18396C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.1053C>T MANE Select ENSP00000242592.4:p.Ala351=
ENST00000242592.8:c.1053C>T ENSP00000242592.4:p.Ala351=
ENST00000411593.2:c.1041C>T ENSP00000401045.2:p.Ala347=
NM_000017.3:c.1053C>T NP_000008.1:p.Ala351=
NM_001302554.1:c.1041C>T NP_001289483.1:p.Ala347=
NM_000017.4:c.1053C>T MANE Select NP_000008.1:p.Ala351=
NM_001302554.2:c.1041C>T NP_001289483.1:p.Ala347=
Search 100 bp 5'
Search 100 bp 3'