Canonical Allele Identifier: CA2245714913
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224621C= , CM000679.2:g.7224621C= GRCh38
NC_000017.10:g.7127940C= , CM000679.1:g.7127940C= GRCh37
NC_000017.9:g.7068664C= NCBI36
NG_007975.1:g.9788C=
NG_008391.2:g.430G=
NG_033038.1:g.14924G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1679-21C= MANE Select ENSP00000349297.5:n.1679-21C=
ENST00000322910.9:c.*1634-21C= ENSP00000325395.5:n.*1634-21C=
ENST00000350303.9:c.1613-21C= ENSP00000344152.5:n.1613-21C=
ENST00000356839.9:c.1679-21C= ENSP00000349297.5:n.1679-21C=
ENST00000542255.6:c.536+69C=
ENST00000543245.6:c.1748-21C= ENSP00000438689.2:n.1748-21C=
ENST00000578319.5:n.260-21C=
ENST00000578711.1:n.1117C=
ENST00000578809.5:n.251-21C=
ENST00000579425.5:n.795-21C=
ENST00000579546.1:c.414-21C=
ENST00000582450.1:n.255C=
ENST00000583074.5:n.299+69C=
ENST00000583848.5:c.65-41C= ENSP00000466487.1:n.65-41C=
ENST00000583850.5:n.450-21C=
ENST00000583858.5:c.610-21C=
ENST00000585203.6:n.870-21C=
NM_000018.3:c.1679-21C= NP_000009.1:n.1679-21C=
NM_001033859.2:c.1613-21C= NP_001029031.1:n.1613-21C=
NM_001270447.1:c.1748-21C= NP_001257376.1:n.1748-21C=
NM_001270448.1:c.1451-21C= NP_001257377.1:n.1451-21C=
XM_006721516.2:c.1678+69C= XP_006721579.2:n.1678+69C=
XM_011523829.1:c.1576+69C= XP_011522131.1:n.1576+69C=
XM_011523830.1:c.1577-21C= XP_011522132.1:n.1577-21C=
XR_934021.1:n.1782-21C=
XR_934022.1:n.1688-21C=
XR_934023.1:n.1687+69C=
XM_006721516.3:c.1678+69C= XP_006721579.2:n.1678+69C=
XM_011523829.2:c.1576+69C= XP_011522131.1:n.1576+69C=
XM_011523830.2:c.1577-21C= XP_011522132.1:n.1577-21C=
XM_024450741.1:c.1667-21C= XP_024306509.1:n.1667-21C=
XR_934021.2:n.1734-21C=
XR_934022.2:n.1640-21C=
XR_934023.2:n.1639+69C=
NM_000018.4:c.1679-21C= MANE Select NP_000009.1:n.1679-21C=
NM_001033859.3:c.1613-21C= NP_001029031.1:n.1613-21C=
NM_001270447.2:c.1748-21C= NP_001257376.1:n.1748-21C=
NM_001270448.2:c.1451-21C= NP_001257377.1:n.1451-21C=