Canonical Allele Identifier: CA2841827568

Gene: ACADVL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7224718A>T , CM000679.2:g.7224718A>T	GRCh38
NC_000017.10:g.7128037A>T , CM000679.1:g.7128037A>T	GRCh37
NC_000017.9:g.7068761A>T	NCBI36
NG_007975.1:g.9885A>T
NG_008391.2:g.333T>A
NG_033038.1:g.14827T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1751+4A>T MANE Select	ENSP00000349297.5:n.1751+4A>T
ENST00000322910.9:c.*1706+4A>T	ENSP00000325395.5:n.*1706+4A>T
ENST00000350303.9:c.1685+4A>T	ENSP00000344152.5:n.1685+4A>T
ENST00000356839.9:c.1751+4A>T	ENSP00000349297.5:n.1751+4A>T
ENST00000542255.6:c.540A>T
ENST00000543245.6:c.1820+4A>T	ENSP00000438689.2:n.1820+4A>T
ENST00000578033.1:n.86A>T
ENST00000578319.5:n.332+4A>T
ENST00000578711.1:n.1214A>T
ENST00000578809.5:n.323+4A>T
ENST00000579425.5:n.867+4A>T
ENST00000579546.1:c.486+4A>T
ENST00000583074.5:n.303A>T
ENST00000583848.5:c.117+4A>T	ENSP00000466487.1:n.117+4A>T
ENST00000583850.5:n.522+4A>T
ENST00000583858.5:c.682+4A>T
ENST00000585203.6:n.942+4A>T
NM_000018.3:c.1751+4A>T	NP_000009.1:n.1751+4A>T
NM_001033859.2:c.1685+4A>T	NP_001029031.1:n.1685+4A>T
NM_001270447.1:c.1820+4A>T	NP_001257376.1:n.1820+4A>T
NM_001270448.1:c.1523+4A>T	NP_001257377.1:n.1523+4A>T
XM_006721516.2:c.1682A>T	XP_006721579.2:p.Glu561Val
XM_011523829.1:c.1580A>T	XP_011522131.1:p.Glu527Val
XM_011523830.1:c.1649+4A>T	XP_011522132.1:n.1649+4A>T
XR_934021.1:n.1854+4A>T
XR_934022.1:n.1760+4A>T
XR_934023.1:n.1691A>T
XM_006721516.3:c.1682A>T	XP_006721579.2:p.Glu561Val
XM_011523829.2:c.1580A>T	XP_011522131.1:p.Glu527Val
XM_011523830.2:c.1649+4A>T	XP_011522132.1:n.1649+4A>T
XM_024450741.1:c.1739+4A>T	XP_024306509.1:n.1739+4A>T
XR_934021.2:n.1806+4A>T
XR_934022.2:n.1712+4A>T
XR_934023.2:n.1643A>T
NM_000018.4:c.1751+4A>T MANE Select	NP_000009.1:n.1751+4A>T
NM_001033859.3:c.1685+4A>T	NP_001029031.1:n.1685+4A>T
NM_001270447.2:c.1820+4A>T	NP_001257376.1:n.1820+4A>T
NM_001270448.2:c.1523+4A>T	NP_001257377.1:n.1523+4A>T