Canonical Allele Identifier: CA2621369646
Gene: ACADS HGNC NCBI

Linked Data

gnomAD v4: 12-120738953-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120738953G>T , CM000674.2:g.120738953G>T GRCh38
NC_000012.11:g.121176756G>T , CM000674.1:g.121176756G>T GRCh37
NC_000012.10:g.119661139G>T NCBI36
NG_007991.1:g.18186G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000242592.9:c.1029+38G>T MANE Select ENSP00000242592.4:n.1029+38G>T
ENST00000242592.8:c.1029+38G>T ENSP00000242592.4:n.1029+38G>T
ENST00000411593.2:c.1017+38G>T ENSP00000401045.2:n.1017+38G>T
NM_000017.3:c.1029+38G>T NP_000008.1:n.1029+38G>T
NM_001302554.1:c.1017+38G>T NP_001289483.1:n.1017+38G>T
NM_000017.4:c.1029+38G>T MANE Select NP_000008.1:n.1029+38G>T
NM_001302554.2:c.1017+38G>T NP_001289483.1:n.1017+38G>T
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