Canonical Allele Identifier: CA2067555434
Gene: ACADS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120738674_120738677delinsATGG , CM000674.2:g.120738674_120738677delinsATGG GRCh38
NC_000012.11:g.121176477_121176480delinsATGG , CM000674.1:g.121176477_121176480delinsATGG GRCh37
NC_000012.10:g.119660860_119660863delinsATGG NCBI36
NG_007991.1:g.17907_17910delinsATGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.933+4_933+7delinsATGG MANE Select ENSP00000242592.4:n.933+4_933+7delinsATGG
ENST00000242592.8:c.933+4_933+7delinsATGG ENSP00000242592.4:n.933+4_933+7delinsATGG
ENST00000411593.2:c.921+4_921+7delinsATGG ENSP00000401045.2:n.921+4_921+7delinsATGG
NM_000017.3:c.933+4_933+7delinsATGG NP_000008.1:n.933+4_933+7delinsATGG
NM_001302554.1:c.921+4_921+7delinsATGG NP_001289483.1:n.921+4_921+7delinsATGG
NM_000017.4:c.933+4_933+7delinsATGG MANE Select NP_000008.1:n.933+4_933+7delinsATGG
NM_001302554.2:c.921+4_921+7delinsATGG NP_001289483.1:n.921+4_921+7delinsATGG