Canonical Allele Identifier: CA244521811
Gene: ACADS HGNC NCBI

Linked Data

dbSNP Id: rs369198779
gnomAD v3: 12-120737229-T-A
gnomAD v4: 12-120737229-T-A
MyVariant Identifiers: chr12:g.121175032T>A (hg19) chr12:g.120737229T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120737229T>A , CM000674.2:g.120737229T>A GRCh38
NC_000012.11:g.121175032T>A , CM000674.1:g.121175032T>A GRCh37
NC_000012.10:g.119659415T>A NCBI36
NG_007991.1:g.16462T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.360+94T>A MANE Select ENSP00000242592.4:n.360+94T>A
ENST00000242592.8:c.360+94T>A ENSP00000242592.4:n.360+94T>A
ENST00000411593.2:c.360+94T>A ENSP00000401045.2:n.360+94T>A
ENST00000539690.1:n.566T>A
NM_000017.3:c.360+94T>A NP_000008.1:n.360+94T>A
NM_001302554.1:c.360+94T>A NP_001289483.1:n.360+94T>A
NM_000017.4:c.360+94T>A MANE Select NP_000008.1:n.360+94T>A
NM_001302554.2:c.360+94T>A NP_001289483.1:n.360+94T>A
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