Canonical Allele Identifier: CA2245714480
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224504_7224505delinsGC , CM000679.2:g.7224504_7224505delinsGC GRCh38
NC_000017.10:g.7127823_7127824delinsGC , CM000679.1:g.7127823_7127824delinsGC GRCh37
NC_000017.9:g.7068547_7068548delinsGC NCBI36
NG_007975.1:g.9671_9672delinsGC
NG_008391.2:g.546_547delinsGC
NG_033038.1:g.15040_15041delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1630_1631delinsGC MANE Select ENSP00000349297.5:p.Ala544=
ENST00000322910.9:c.*1585_*1586delinsGC ENSP00000325395.5:n.*1585_*1586delinsGC
ENST00000350303.9:c.1564_1565delinsGC ENSP00000344152.5:p.Ala522=
ENST00000356839.9:c.1630_1631delinsGC ENSP00000349297.5:p.Ala544=
ENST00000542255.6:c.488_489delinsGC
ENST00000543245.6:c.1699_1700delinsGC ENSP00000438689.2:p.Ala567=
ENST00000578319.5:n.211_212delinsGC
ENST00000578711.1:n.1000_1001delinsGC
ENST00000578809.5:n.202_203delinsGC
ENST00000579391.1:n.234_235delinsGC
ENST00000579425.5:n.746_747delinsGC
ENST00000579546.1:c.365_366delinsGC
ENST00000579894.5:n.417_418delinsGC
ENST00000582450.1:n.138_139delinsGC
ENST00000583074.5:n.251_252delinsGC
ENST00000583848.5:c.16_17delinsGC ENSP00000466487.1:p.Ala6=
ENST00000583850.5:n.401_402delinsGC
ENST00000583858.5:c.561_562delinsGC
ENST00000585203.6:n.821_822delinsGC
NM_000018.3:c.1630_1631delinsGC NP_000009.1:p.Ala544=
NM_001033859.2:c.1564_1565delinsGC NP_001029031.1:p.Ala522=
NM_001270447.1:c.1699_1700delinsGC NP_001257376.1:p.Ala567=
NM_001270448.1:c.1402_1403delinsGC NP_001257377.1:p.Ala468=
XM_006721516.2:c.1630_1631delinsGC XP_006721579.2:p.Ala544=
XM_011523829.1:c.1528_1529delinsGC XP_011522131.1:p.Ala510=
XM_011523830.1:c.1528_1529delinsGC XP_011522132.1:p.Ala510=
XR_934021.1:n.1733_1734delinsGC
XR_934022.1:n.1639_1640delinsGC
XR_934023.1:n.1639_1640delinsGC
XM_006721516.3:c.1630_1631delinsGC XP_006721579.2:p.Ala544=
XM_011523829.2:c.1528_1529delinsGC XP_011522131.1:p.Ala510=
XM_011523830.2:c.1528_1529delinsGC XP_011522132.1:p.Ala510=
XM_024450741.1:c.1618_1619delinsGC XP_024306509.1:p.Ala540=
XR_934021.2:n.1685_1686delinsGC
XR_934022.2:n.1591_1592delinsGC
XR_934023.2:n.1591_1592delinsGC
NM_000018.4:c.1630_1631delinsGC MANE Select NP_000009.1:p.Ala544=
NM_001033859.3:c.1564_1565delinsGC NP_001029031.1:p.Ala522=
NM_001270447.2:c.1699_1700delinsGC NP_001257376.1:p.Ala567=
NM_001270448.2:c.1402_1403delinsGC NP_001257377.1:p.Ala468=