Canonical Allele Identifier: CA2245714975
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224632T= , CM000679.2:g.7224632T= GRCh38
NC_000017.10:g.7127951T= , CM000679.1:g.7127951T= GRCh37
NC_000017.9:g.7068675T= NCBI36
NG_007975.1:g.9799T=
NG_008391.2:g.419A=
NG_033038.1:g.14913A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1679-10T= MANE Select ENSP00000349297.5:n.1679-10T=
ENST00000322910.9:c.*1634-10T= ENSP00000325395.5:n.*1634-10T=
ENST00000350303.9:c.1613-10T= ENSP00000344152.5:n.1613-10T=
ENST00000356839.9:c.1679-10T= ENSP00000349297.5:n.1679-10T=
ENST00000542255.6:c.536+80T=
ENST00000543245.6:c.1748-10T= ENSP00000438689.2:n.1748-10T=
ENST00000578319.5:n.260-10T=
ENST00000578711.1:n.1128T=
ENST00000578809.5:n.251-10T=
ENST00000579425.5:n.795-10T=
ENST00000579546.1:c.414-10T=
ENST00000582450.1:n.266T=
ENST00000583074.5:n.299+80T=
ENST00000583848.5:c.65-30T= ENSP00000466487.1:n.65-30T=
ENST00000583850.5:n.450-10T=
ENST00000583858.5:c.610-10T=
ENST00000585203.6:n.870-10T=
NM_000018.3:c.1679-10T= NP_000009.1:n.1679-10T=
NM_001033859.2:c.1613-10T= NP_001029031.1:n.1613-10T=
NM_001270447.1:c.1748-10T= NP_001257376.1:n.1748-10T=
NM_001270448.1:c.1451-10T= NP_001257377.1:n.1451-10T=
XM_006721516.2:c.1678+80T= XP_006721579.2:n.1678+80T=
XM_011523829.1:c.1576+80T= XP_011522131.1:n.1576+80T=
XM_011523830.1:c.1577-10T= XP_011522132.1:n.1577-10T=
XR_934021.1:n.1782-10T=
XR_934022.1:n.1688-10T=
XR_934023.1:n.1687+80T=
XM_006721516.3:c.1678+80T= XP_006721579.2:n.1678+80T=
XM_011523829.2:c.1576+80T= XP_011522131.1:n.1576+80T=
XM_011523830.2:c.1577-10T= XP_011522132.1:n.1577-10T=
XM_024450741.1:c.1667-10T= XP_024306509.1:n.1667-10T=
XR_934021.2:n.1734-10T=
XR_934022.2:n.1640-10T=
XR_934023.2:n.1639+80T=
NM_000018.4:c.1679-10T= MANE Select NP_000009.1:n.1679-10T=
NM_001033859.3:c.1613-10T= NP_001029031.1:n.1613-10T=
NM_001270447.2:c.1748-10T= NP_001257376.1:n.1748-10T=
NM_001270448.2:c.1451-10T= NP_001257377.1:n.1451-10T=