Canonical Allele Identifier: CA2635786346
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224639dup , CM000679.2:g.7224639dup GRCh38
NC_000017.10:g.7127958dup , CM000679.1:g.7127958dup GRCh37
NC_000017.9:g.7068682dup NCBI36
NG_007975.1:g.9806dup
NG_008391.2:g.412dup
NG_033038.1:g.14906dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1679-3dup MANE Select ENSP00000349297.5:n.1679-3dup
ENST00000322910.9:c.*1634-3dup ENSP00000325395.5:n.*1634-3dup
ENST00000350303.9:c.1613-3dup ENSP00000344152.5:n.1613-3dup
ENST00000356839.9:c.1679-3dup ENSP00000349297.5:n.1679-3dup
ENST00000542255.6:c.537-76dup
ENST00000543245.6:c.1748-3dup ENSP00000438689.2:n.1748-3dup
ENST00000578033.1:n.7dup
ENST00000578319.5:n.260-3dup
ENST00000578711.1:n.1135dup
ENST00000578809.5:n.251-3dup
ENST00000579425.5:n.795-3dup
ENST00000579546.1:c.414-3dup
ENST00000582450.1:n.273dup
ENST00000583074.5:n.300-76dup
ENST00000583848.5:c.65-23dup ENSP00000466487.1:n.65-23dup
ENST00000583850.5:n.450-3dup
ENST00000583858.5:c.610-3dup
ENST00000585203.6:n.870-3dup
NM_000018.3:c.1679-3dup NP_000009.1:n.1679-3dup
NM_001033859.2:c.1613-3dup NP_001029031.1:n.1613-3dup
NM_001270447.1:c.1748-3dup NP_001257376.1:n.1748-3dup
NM_001270448.1:c.1451-3dup NP_001257377.1:n.1451-3dup
XM_006721516.2:c.1679-76dup XP_006721579.2:n.1679-76dup
XM_011523829.1:c.1577-76dup XP_011522131.1:n.1577-76dup
XM_011523830.1:c.1577-3dup XP_011522132.1:n.1577-3dup
XR_934021.1:n.1782-3dup
XR_934022.1:n.1688-3dup
XR_934023.1:n.1688-76dup
XM_006721516.3:c.1679-76dup XP_006721579.2:n.1679-76dup
XM_011523829.2:c.1577-76dup XP_011522131.1:n.1577-76dup
XM_011523830.2:c.1577-3dup XP_011522132.1:n.1577-3dup
XM_024450741.1:c.1667-3dup XP_024306509.1:n.1667-3dup
XR_934021.2:n.1734-3dup
XR_934022.2:n.1640-3dup
XR_934023.2:n.1640-76dup
NM_000018.4:c.1679-3dup MANE Select NP_000009.1:n.1679-3dup
NM_001033859.3:c.1613-3dup NP_001029031.1:n.1613-3dup
NM_001270447.2:c.1748-3dup NP_001257376.1:n.1748-3dup
NM_001270448.2:c.1451-3dup NP_001257377.1:n.1451-3dup