Canonical Allele Identifier: CA2621366698
Gene: ACADS HGNC NCBI

Linked Data

gnomAD v4: 12-120737157-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120737157T>G , CM000674.2:g.120737157T>G GRCh38
NC_000012.11:g.121174960T>G , CM000674.1:g.121174960T>G GRCh37
NC_000012.10:g.119659343T>G NCBI36
NG_007991.1:g.16390T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.360+22T>G MANE Select ENSP00000242592.4:n.360+22T>G
ENST00000242592.8:c.360+22T>G ENSP00000242592.4:n.360+22T>G
ENST00000411593.2:c.360+22T>G ENSP00000401045.2:n.360+22T>G
ENST00000539690.1:n.494T>G
NM_000017.3:c.360+22T>G NP_000008.1:n.360+22T>G
NM_001302554.1:c.360+22T>G NP_001289483.1:n.360+22T>G
NM_000017.4:c.360+22T>G MANE Select NP_000008.1:n.360+22T>G
NM_001302554.2:c.360+22T>G NP_001289483.1:n.360+22T>G
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