Canonical Allele Identifier: CA2067555749
Gene: ACADS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120739220_120739221delinsAG , CM000674.2:g.120739220_120739221delinsAG GRCh38
NC_000012.11:g.121177023_121177024delinsAG , CM000674.1:g.121177023_121177024delinsAG GRCh37
NC_000012.10:g.119661406_119661407delinsAG NCBI36
NG_007991.1:g.18453_18454delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.1086+24_1086+25delinsAG MANE Select ENSP00000242592.4:n.1086+24_1086+25delinsAG
ENST00000242592.8:c.1086+24_1086+25delinsAG ENSP00000242592.4:n.1086+24_1086+25delinsAG
ENST00000411593.2:c.1074+24_1074+25delinsAG ENSP00000401045.2:n.1074+24_1074+25delinsAG
NM_000017.3:c.1086+24_1086+25delinsAG NP_000008.1:n.1086+24_1086+25delinsAG
NM_001302554.1:c.1074+24_1074+25delinsAG NP_001289483.1:n.1074+24_1074+25delinsAG
NM_000017.4:c.1086+24_1086+25delinsAG MANE Select NP_000008.1:n.1086+24_1086+25delinsAG
NM_001302554.2:c.1074+24_1074+25delinsAG NP_001289483.1:n.1074+24_1074+25delinsAG