Canonical Allele Identifier: CA774742171
Gene: ACADVL HGNC NCBI

Linked Data

dbSNP Id: rs1331138634

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221821_7221823del , CM000679.2:g.7221821_7221823del GRCh38
NC_000017.10:g.7125140_7125142del , CM000679.1:g.7125140_7125142del GRCh37
NC_000017.9:g.7065864_7065866del NCBI36
NG_007975.1:g.6988_6990del
NG_008391.2:g.3229_3231del

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.623-131_623-129del MANE Select ENSP00000349297.5:n.623-131_623-129del
ENST00000322910.9:c.*578-131_*578-129del ENSP00000325395.5:n.*578-131_*578-129del
ENST00000350303.9:c.557-131_557-129del ENSP00000344152.5:n.557-131_557-129del
ENST00000356839.9:c.623-131_623-129del ENSP00000349297.5:n.623-131_623-129del
ENST00000543245.6:c.692-131_692-129del ENSP00000438689.2:n.692-131_692-129del
ENST00000577191.5:n.700-131_700-129del
ENST00000577857.5:n.439-131_439-129del
ENST00000579286.5:n.804-131_804-129del
ENST00000579886.2:c.461-131_461-129del ENSP00000463246.1:n.461-131_461-129del
ENST00000580365.1:n.354-131_354-129del
ENST00000581378.5:c.341-131_341-129del
ENST00000581562.5:n.525-131_525-129del
ENST00000583312.5:c.623-116_623-114del ENSP00000467920.1:n.623-116_623-114del
ENST00000583760.1:n.405-131_405-129del
NM_000018.3:c.623-131_623-129del NP_000009.1:n.623-131_623-129del
NM_001033859.2:c.557-131_557-129del NP_001029031.1:n.557-131_557-129del
NM_001270447.1:c.692-131_692-129del NP_001257376.1:n.692-131_692-129del
NM_001270448.1:c.395-131_395-129del NP_001257377.1:n.395-131_395-129del
XM_006721516.2:c.623-131_623-129del XP_006721579.2:n.623-131_623-129del
XM_011523829.1:c.623-131_623-129del XP_011522131.1:n.623-131_623-129del
XM_011523830.1:c.623-131_623-129del XP_011522132.1:n.623-131_623-129del
XR_934021.1:n.730-131_730-129del
XR_934022.1:n.730-131_730-129del
XR_934023.1:n.730-131_730-129del
XM_006721516.3:c.623-131_623-129del XP_006721579.2:n.623-131_623-129del
XM_011523829.2:c.623-131_623-129del XP_011522131.1:n.623-131_623-129del
XM_011523830.2:c.623-131_623-129del XP_011522132.1:n.623-131_623-129del
XM_024450741.1:c.623-131_623-129del XP_024306509.1:n.623-131_623-129del
XR_934021.2:n.682-131_682-129del
XR_934022.2:n.682-131_682-129del
XR_934023.2:n.682-131_682-129del
NM_000018.4:c.623-131_623-129del MANE Select NP_000009.1:n.623-131_623-129del
NM_001033859.3:c.557-131_557-129del NP_001029031.1:n.557-131_557-129del
NM_001270447.2:c.692-131_692-129del NP_001257376.1:n.692-131_692-129del
NM_001270448.2:c.395-131_395-129del NP_001257377.1:n.395-131_395-129del