Canonical Allele Identifier: CA2245700097
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221559G= , CM000679.2:g.7221559G= GRCh38
NC_000017.10:g.7124878G= , CM000679.1:g.7124878G= GRCh37
NC_000017.9:g.7065602G= NCBI36
NG_007975.1:g.6726G=
NG_008391.2:g.3492C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.499G= MANE Select ENSP00000349297.5:p.Val167=
ENST00000322910.9:c.*454G= ENSP00000325395.5:n.*454G=
ENST00000350303.9:c.433G= ENSP00000344152.5:p.Val145=
ENST00000356839.9:c.499G= ENSP00000349297.5:p.Val167=
ENST00000543245.6:c.568G= ENSP00000438689.2:p.Val190=
ENST00000577191.5:n.576G=
ENST00000577433.5:n.707G=
ENST00000577857.5:n.315G=
ENST00000579286.5:n.680G=
ENST00000579886.2:c.337G= ENSP00000463246.1:p.Val113=
ENST00000580365.1:n.230G=
ENST00000581378.5:c.217G=
ENST00000581562.5:n.525-393G=
ENST00000582166.1:n.480G=
ENST00000583312.5:c.499G= ENSP00000467920.1:p.Val167=
ENST00000583760.1:n.281G=
NM_000018.3:c.499G= NP_000009.1:p.Val167=
NM_001033859.2:c.433G= NP_001029031.1:p.Val145=
NM_001270447.1:c.568G= NP_001257376.1:p.Val190=
NM_001270448.1:c.271G= NP_001257377.1:p.Val91=
XM_006721516.2:c.499G= XP_006721579.2:p.Val167=
XM_011523829.1:c.499G= XP_011522131.1:p.Val167=
XM_011523830.1:c.499G= XP_011522132.1:p.Val167=
XR_934021.1:n.606G=
XR_934022.1:n.606G=
XR_934023.1:n.606G=
XM_006721516.3:c.499G= XP_006721579.2:p.Val167=
XM_011523829.2:c.499G= XP_011522131.1:p.Val167=
XM_011523830.2:c.499G= XP_011522132.1:p.Val167=
XM_024450741.1:c.499G= XP_024306509.1:p.Val167=
XR_934021.2:n.558G=
XR_934022.2:n.558G=
XR_934023.2:n.558G=
NM_000018.4:c.499G= MANE Select NP_000009.1:p.Val167=
NM_001033859.3:c.433G= NP_001029031.1:p.Val145=
NM_001270447.2:c.568G= NP_001257376.1:p.Val190=
NM_001270448.2:c.271G= NP_001257377.1:p.Val91=