Canonical Allele Identifier: CA981153031
Gene: ACADVL HGNC NCBI

Linked Data

dbSNP Id: rs2071259972
gnomAD v3: 17-7222108-C-T
gnomAD v4: 17-7222108-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222108C>T , CM000679.2:g.7222108C>T GRCh38
NC_000017.10:g.7125427C>T , CM000679.1:g.7125427C>T GRCh37
NC_000017.9:g.7066151C>T NCBI36
NG_007975.1:g.7275C>T
NG_008391.2:g.2943G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.752+27C>T MANE Select ENSP00000349297.5:n.752+27C>T
ENST00000322910.9:c.*707+27C>T ENSP00000325395.5:n.*707+27C>T
ENST00000350303.9:c.686+27C>T ENSP00000344152.5:n.686+27C>T
ENST00000356839.9:c.752+27C>T ENSP00000349297.5:n.752+27C>T
ENST00000543245.6:c.821+27C>T ENSP00000438689.2:n.821+27C>T
ENST00000577191.5:n.856C>T
ENST00000581378.5:c.470+27C>T
ENST00000582379.1:n.136+27C>T
ENST00000583760.1:n.561C>T
NM_000018.3:c.752+27C>T NP_000009.1:n.752+27C>T
NM_001033859.2:c.686+27C>T NP_001029031.1:n.686+27C>T
NM_001270447.1:c.821+27C>T NP_001257376.1:n.821+27C>T
NM_001270448.1:c.524+27C>T NP_001257377.1:n.524+27C>T
XM_006721516.2:c.752+27C>T XP_006721579.2:n.752+27C>T
XM_011523829.1:c.752+27C>T XP_011522131.1:n.752+27C>T
XM_011523830.1:c.752+27C>T XP_011522132.1:n.752+27C>T
XR_934021.1:n.859+27C>T
XR_934022.1:n.859+27C>T
XR_934023.1:n.859+27C>T
XM_006721516.3:c.752+27C>T XP_006721579.2:n.752+27C>T
XM_011523829.2:c.752+27C>T XP_011522131.1:n.752+27C>T
XM_011523830.2:c.752+27C>T XP_011522132.1:n.752+27C>T
XM_024450741.1:c.752+27C>T XP_024306509.1:n.752+27C>T
XR_934021.2:n.811+27C>T
XR_934022.2:n.811+27C>T
XR_934023.2:n.811+27C>T
NM_000018.4:c.752+27C>T MANE Select NP_000009.1:n.752+27C>T
NM_001033859.3:c.686+27C>T NP_001029031.1:n.686+27C>T
NM_001270447.2:c.821+27C>T NP_001257376.1:n.821+27C>T
NM_001270448.2:c.524+27C>T NP_001257377.1:n.524+27C>T
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