Canonical Allele Identifier: CA6831223
Gene: ACADS HGNC NCBI

Linked Data

dbSNP Id: rs751738987
ExAC: 12:121177118 G / A
gnomAD v2: 12-121177118-G-A
COSMIC: COSM5913317
MyVariant Identifiers: chr12:g.121177118G>A (hg19) chr12:g.120739315G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120739315G>A , CM000674.2:g.120739315G>A GRCh38
NC_000012.11:g.121177118G>A , CM000674.1:g.121177118G>A GRCh37
NC_000012.10:g.119661501G>A NCBI36
NG_007991.1:g.18548G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.1106G>A MANE Select ENSP00000242592.4:p.Gly369Asp
ENST00000242592.8:c.1106G>A ENSP00000242592.4:p.Gly369Asp
ENST00000411593.2:c.1094G>A ENSP00000401045.2:p.Gly365Asp
NM_000017.3:c.1106G>A NP_000008.1:p.Gly369Asp
NM_001302554.1:c.1094G>A NP_001289483.1:p.Gly365Asp
NM_000017.4:c.1106G>A MANE Select NP_000008.1:p.Gly369Asp
NM_001302554.2:c.1094G>A NP_001289483.1:p.Gly365Asp
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