Canonical Allele Identifier: CA2245711786
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7223744C= , CM000679.2:g.7223744C= GRCh38
NC_000017.10:g.7127063C= , CM000679.1:g.7127063C= GRCh37
NC_000017.9:g.7067787C= NCBI36
NG_007975.1:g.8911C=
NG_008391.2:g.1307G=
NG_033038.1:g.15801G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1269+14C= MANE Select ENSP00000349297.5:n.1269+14C=
ENST00000322910.9:c.*1224+14C= ENSP00000325395.5:n.*1224+14C=
ENST00000350303.9:c.1203+14C= ENSP00000344152.5:n.1203+14C=
ENST00000356839.9:c.1269+14C= ENSP00000349297.5:n.1269+14C=
ENST00000542255.6:c.127+14C=
ENST00000543245.6:c.1338+14C= ENSP00000438689.2:n.1338+14C=
ENST00000578579.2:n.440+14C=
ENST00000578711.1:n.240C=
ENST00000578824.5:n.685+14C=
ENST00000579425.5:n.293+14C=
ENST00000579546.1:c.106+14C=
ENST00000583850.5:n.44+14C=
ENST00000583858.5:c.298+14C=
ENST00000585203.6:n.477+14C=
NM_000018.3:c.1269+14C= NP_000009.1:n.1269+14C=
NM_001033859.2:c.1203+14C= NP_001029031.1:n.1203+14C=
NM_001270447.1:c.1338+14C= NP_001257376.1:n.1338+14C=
NM_001270448.1:c.1041+14C= NP_001257377.1:n.1041+14C=
XM_006721516.2:c.1269+14C= XP_006721579.2:n.1269+14C=
XM_011523829.1:c.1269+14C= XP_011522131.1:n.1269+14C=
XM_011523830.1:c.1269+14C= XP_011522132.1:n.1269+14C=
XR_934021.1:n.1376+14C=
XR_934022.1:n.1376+14C=
XR_934023.1:n.1376+14C=
XM_006721516.3:c.1269+14C= XP_006721579.2:n.1269+14C=
XM_011523829.2:c.1269+14C= XP_011522131.1:n.1269+14C=
XM_011523830.2:c.1269+14C= XP_011522132.1:n.1269+14C=
XM_024450741.1:c.1269+14C= XP_024306509.1:n.1269+14C=
XR_934021.2:n.1328+14C=
XR_934022.2:n.1328+14C=
XR_934023.2:n.1328+14C=
NM_000018.4:c.1269+14C= MANE Select NP_000009.1:n.1269+14C=
NM_001033859.3:c.1203+14C= NP_001029031.1:n.1203+14C=
NM_001270447.2:c.1338+14C= NP_001257376.1:n.1338+14C=
NM_001270448.2:c.1041+14C= NP_001257377.1:n.1041+14C=