Canonical Allele Identifier: CA2245714528
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224524G= , CM000679.2:g.7224524G= GRCh38
NC_000017.10:g.7127843G= , CM000679.1:g.7127843G= GRCh37
NC_000017.9:g.7068567G= NCBI36
NG_007975.1:g.9691G=
NG_008391.2:g.527C=
NG_033038.1:g.15021C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1650G= MANE Select ENSP00000349297.5:p.Lys550=
ENST00000322910.9:c.*1605G= ENSP00000325395.5:n.*1605G=
ENST00000350303.9:c.1584G= ENSP00000344152.5:p.Lys528=
ENST00000356839.9:c.1650G= ENSP00000349297.5:p.Lys550=
ENST00000542255.6:c.508G=
ENST00000543245.6:c.1719G= ENSP00000438689.2:p.Lys573=
ENST00000578319.5:n.231G=
ENST00000578711.1:n.1020G=
ENST00000578809.5:n.222G=
ENST00000579391.1:n.254G=
ENST00000579425.5:n.766G=
ENST00000579546.1:c.385G=
ENST00000582450.1:n.158G=
ENST00000583074.5:n.271G=
ENST00000583848.5:c.36G= ENSP00000466487.1:p.Lys12=
ENST00000583850.5:n.421G=
ENST00000583858.5:c.581G=
ENST00000585203.6:n.841G=
NM_000018.3:c.1650G= NP_000009.1:p.Lys550=
NM_001033859.2:c.1584G= NP_001029031.1:p.Lys528=
NM_001270447.1:c.1719G= NP_001257376.1:p.Lys573=
NM_001270448.1:c.1422G= NP_001257377.1:p.Lys474=
XM_006721516.2:c.1650G= XP_006721579.2:p.Lys550=
XM_011523829.1:c.1548G= XP_011522131.1:p.Lys516=
XM_011523830.1:c.1548G= XP_011522132.1:p.Lys516=
XR_934021.1:n.1753G=
XR_934022.1:n.1659G=
XR_934023.1:n.1659G=
XM_006721516.3:c.1650G= XP_006721579.2:p.Lys550=
XM_011523829.2:c.1548G= XP_011522131.1:p.Lys516=
XM_011523830.2:c.1548G= XP_011522132.1:p.Lys516=
XM_024450741.1:c.1638G= XP_024306509.1:p.Lys546=
XR_934021.2:n.1705G=
XR_934022.2:n.1611G=
XR_934023.2:n.1611G=
NM_000018.4:c.1650G= MANE Select NP_000009.1:p.Lys550=
NM_001033859.3:c.1584G= NP_001029031.1:p.Lys528=
NM_001270447.2:c.1719G= NP_001257376.1:p.Lys573=
NM_001270448.2:c.1422G= NP_001257377.1:p.Lys474=