Canonical Allele Identifier: CA2245715009
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224637G= , CM000679.2:g.7224637G= GRCh38
NC_000017.10:g.7127956G= , CM000679.1:g.7127956G= GRCh37
NC_000017.9:g.7068680G= NCBI36
NG_007975.1:g.9804G=
NG_008391.2:g.414C=
NG_033038.1:g.14908C=

Transcript Alleles

HGVS Amino-acid change
ENST00000356839.10:c.1679-5G= MANE Select ENSP00000349297.5:n.1679-5G=
ENST00000322910.9:c.*1634-5G= ENSP00000325395.5:n.*1634-5G=
ENST00000350303.9:c.1613-5G= ENSP00000344152.5:n.1613-5G=
ENST00000356839.9:c.1679-5G= ENSP00000349297.5:n.1679-5G=
ENST00000542255.6:c.537-78G=
ENST00000543245.6:c.1748-5G= ENSP00000438689.2:n.1748-5G=
ENST00000578033.1:n.5G=
ENST00000578319.5:n.260-5G=
ENST00000578711.1:n.1133G=
ENST00000578809.5:n.251-5G=
ENST00000579425.5:n.795-5G=
ENST00000579546.1:c.414-5G=
ENST00000582450.1:n.271G=
ENST00000583074.5:n.300-78G=
ENST00000583848.5:c.65-25G= ENSP00000466487.1:n.65-25G=
ENST00000583850.5:n.450-5G=
ENST00000583858.5:c.610-5G=
ENST00000585203.6:n.870-5G=
NM_000018.3:c.1679-5G= NP_000009.1:n.1679-5G=
NM_001033859.2:c.1613-5G= NP_001029031.1:n.1613-5G=
NM_001270447.1:c.1748-5G= NP_001257376.1:n.1748-5G=
NM_001270448.1:c.1451-5G= NP_001257377.1:n.1451-5G=
XM_006721516.2:c.1679-78G= XP_006721579.2:n.1679-78G=
XM_011523829.1:c.1577-78G= XP_011522131.1:n.1577-78G=
XM_011523830.1:c.1577-5G= XP_011522132.1:n.1577-5G=
XR_934021.1:n.1782-5G=
XR_934022.1:n.1688-5G=
XR_934023.1:n.1688-78G=
XM_006721516.3:c.1679-78G= XP_006721579.2:n.1679-78G=
XM_011523829.2:c.1577-78G= XP_011522131.1:n.1577-78G=
XM_011523830.2:c.1577-5G= XP_011522132.1:n.1577-5G=
XM_024450741.1:c.1667-5G= XP_024306509.1:n.1667-5G=
XR_934021.2:n.1734-5G=
XR_934022.2:n.1640-5G=
XR_934023.2:n.1640-78G=
NM_000018.4:c.1679-5G= MANE Select NP_000009.1:n.1679-5G=
NM_001033859.3:c.1613-5G= NP_001029031.1:n.1613-5G=
NM_001270447.2:c.1748-5G= NP_001257376.1:n.1748-5G=
NM_001270448.2:c.1451-5G= NP_001257377.1:n.1451-5G=