Canonical Allele Identifier: CA2621369069
Gene: ACADS HGNC NCBI

Linked Data

gnomAD v4: 12-120738794-TGTG-T
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120738798_120738800del , CM000674.2:g.120738798_120738800del GRCh38
NC_000012.11:g.121176601_121176603del , CM000674.1:g.121176601_121176603del GRCh37
NC_000012.10:g.119660984_119660986del NCBI36
NG_007991.1:g.18031_18033del

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.934-22_934-20del MANE Select ENSP00000242592.4:n.934-22_934-20del
ENST00000242592.8:c.934-22_934-20del ENSP00000242592.4:n.934-22_934-20del
ENST00000411593.2:c.922-22_922-20del ENSP00000401045.2:n.922-22_922-20del
NM_000017.3:c.934-22_934-20del NP_000008.1:n.934-22_934-20del
NM_001302554.1:c.922-22_922-20del NP_001289483.1:n.922-22_922-20del
NM_000017.4:c.934-22_934-20del MANE Select NP_000008.1:n.934-22_934-20del
NM_001302554.2:c.922-22_922-20del NP_001289483.1:n.922-22_922-20del
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