Canonical Allele Identifier: CA2245714500
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224513G= , CM000679.2:g.7224513G= GRCh38
NC_000017.10:g.7127832G= , CM000679.1:g.7127832G= GRCh37
NC_000017.9:g.7068556G= NCBI36
NG_007975.1:g.9680G=
NG_008391.2:g.538C=
NG_033038.1:g.15032C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1639G= MANE Select ENSP00000349297.5:p.Val547=
ENST00000322910.9:c.*1594G= ENSP00000325395.5:n.*1594G=
ENST00000350303.9:c.1573G= ENSP00000344152.5:p.Val525=
ENST00000356839.9:c.1639G= ENSP00000349297.5:p.Val547=
ENST00000542255.6:c.497G=
ENST00000543245.6:c.1708G= ENSP00000438689.2:p.Val570=
ENST00000578319.5:n.220G=
ENST00000578711.1:n.1009G=
ENST00000578809.5:n.211G=
ENST00000579391.1:n.243G=
ENST00000579425.5:n.755G=
ENST00000579546.1:c.374G=
ENST00000579894.5:n.426G=
ENST00000582450.1:n.147G=
ENST00000583074.5:n.260G=
ENST00000583848.5:c.25G= ENSP00000466487.1:p.Val9=
ENST00000583850.5:n.410G=
ENST00000583858.5:c.570G=
ENST00000585203.6:n.830G=
NM_000018.3:c.1639G= NP_000009.1:p.Val547=
NM_001033859.2:c.1573G= NP_001029031.1:p.Val525=
NM_001270447.1:c.1708G= NP_001257376.1:p.Val570=
NM_001270448.1:c.1411G= NP_001257377.1:p.Val471=
XM_006721516.2:c.1639G= XP_006721579.2:p.Val547=
XM_011523829.1:c.1537G= XP_011522131.1:p.Val513=
XM_011523830.1:c.1537G= XP_011522132.1:p.Val513=
XR_934021.1:n.1742G=
XR_934022.1:n.1648G=
XR_934023.1:n.1648G=
XM_006721516.3:c.1639G= XP_006721579.2:p.Val547=
XM_011523829.2:c.1537G= XP_011522131.1:p.Val513=
XM_011523830.2:c.1537G= XP_011522132.1:p.Val513=
XM_024450741.1:c.1627G= XP_024306509.1:p.Val543=
XR_934021.2:n.1694G=
XR_934022.2:n.1600G=
XR_934023.2:n.1600G=
NM_000018.4:c.1639G= MANE Select NP_000009.1:p.Val547=
NM_001033859.3:c.1573G= NP_001029031.1:p.Val525=
NM_001270447.2:c.1708G= NP_001257376.1:p.Val570=
NM_001270448.2:c.1411G= NP_001257377.1:p.Val471=