Canonical Allele Identifier: CA2245701166
Gene: ACADVL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222151G= , CM000679.2:g.7222151G= GRCh38
NC_000017.10:g.7125470G= , CM000679.1:g.7125470G= GRCh37
NC_000017.9:g.7066194G= NCBI36
NG_007975.1:g.7318G=
NG_008391.2:g.2900C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.753-26G= MANE Select ENSP00000349297.5:n.753-26G=
ENST00000322910.9:c.*708-26G= ENSP00000325395.5:n.*708-26G=
ENST00000350303.9:c.687-26G= ENSP00000344152.5:n.687-26G=
ENST00000356839.9:c.753-26G= ENSP00000349297.5:n.753-26G=
ENST00000543245.6:c.822-26G= ENSP00000438689.2:n.822-26G=
ENST00000577191.5:n.899G=
ENST00000581378.5:c.471-26G=
ENST00000582379.1:n.137-26G=
NM_000018.3:c.753-26G= NP_000009.1:n.753-26G=
NM_001033859.2:c.687-26G= NP_001029031.1:n.687-26G=
NM_001270447.1:c.822-26G= NP_001257376.1:n.822-26G=
NM_001270448.1:c.525-26G= NP_001257377.1:n.525-26G=
XM_006721516.2:c.753-26G= XP_006721579.2:n.753-26G=
XM_011523829.1:c.753-26G= XP_011522131.1:n.753-26G=
XM_011523830.1:c.753-26G= XP_011522132.1:n.753-26G=
XR_934021.1:n.860-26G=
XR_934022.1:n.860-26G=
XR_934023.1:n.860-26G=
XM_006721516.3:c.753-26G= XP_006721579.2:n.753-26G=
XM_011523829.2:c.753-26G= XP_011522131.1:n.753-26G=
XM_011523830.2:c.753-26G= XP_011522132.1:n.753-26G=
XM_024450741.1:c.753-26G= XP_024306509.1:n.753-26G=
XR_934021.2:n.812-26G=
XR_934022.2:n.812-26G=
XR_934023.2:n.812-26G=
NM_000018.4:c.753-26G= MANE Select NP_000009.1:n.753-26G=
NM_001033859.3:c.687-26G= NP_001029031.1:n.687-26G=
NM_001270447.2:c.822-26G= NP_001257376.1:n.822-26G=
NM_001270448.2:c.525-26G= NP_001257377.1:n.525-26G=
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