Canonical Allele Identifier: CA2808367636

Gene: ACADVL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7224754C>G , CM000679.2:g.7224754C>G	GRCh38
NC_000017.10:g.7128073C>G , CM000679.1:g.7128073C>G	GRCh37
NC_000017.9:g.7068797C>G	NCBI36
NG_007975.1:g.9921C>G
NG_008391.2:g.297G>C
NG_033038.1:g.14791G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1751+40C>G MANE Select	ENSP00000349297.5:n.1751+40C>G
ENST00000322910.9:c.*1706+40C>G	ENSP00000325395.5:n.*1706+40C>G
ENST00000350303.9:c.1685+40C>G	ENSP00000344152.5:n.1685+40C>G
ENST00000356839.9:c.1751+40C>G	ENSP00000349297.5:n.1751+40C>G
ENST00000542255.6:c.576C>G
ENST00000543245.6:c.1820+40C>G	ENSP00000438689.2:n.1820+40C>G
ENST00000578033.1:n.122C>G
ENST00000578319.5:n.332+40C>G
ENST00000578711.1:n.1250C>G
ENST00000578809.5:n.323+40C>G
ENST00000579425.5:n.867+40C>G
ENST00000579546.1:c.486+40C>G
ENST00000583074.5:n.339C>G
ENST00000583848.5:c.117+40C>G	ENSP00000466487.1:n.117+40C>G
ENST00000583850.5:n.522+40C>G
ENST00000583858.5:c.682+40C>G
ENST00000585203.6:n.942+40C>G
NM_000018.3:c.1751+40C>G	NP_000009.1:n.1751+40C>G
NM_001033859.2:c.1685+40C>G	NP_001029031.1:n.1685+40C>G
NM_001270447.1:c.1820+40C>G	NP_001257376.1:n.1820+40C>G
NM_001270448.1:c.1523+40C>G	NP_001257377.1:n.1523+40C>G
XM_006721516.2:c.1718C>G	XP_006721579.2:p.Pro573Arg
XM_011523829.1:c.1616C>G	XP_011522131.1:p.Pro539Arg
XM_011523830.1:c.1649+40C>G	XP_011522132.1:n.1649+40C>G
XR_934021.1:n.1854+40C>G
XR_934022.1:n.1760+40C>G
XR_934023.1:n.1727C>G
XM_006721516.3:c.1718C>G	XP_006721579.2:p.Pro573Arg
XM_011523829.2:c.1616C>G	XP_011522131.1:p.Pro539Arg
XM_011523830.2:c.1649+40C>G	XP_011522132.1:n.1649+40C>G
XM_024450741.1:c.1739+40C>G	XP_024306509.1:n.1739+40C>G
XR_934021.2:n.1806+40C>G
XR_934022.2:n.1712+40C>G
XR_934023.2:n.1679C>G
NM_000018.4:c.1751+40C>G MANE Select	NP_000009.1:n.1751+40C>G
NM_001033859.3:c.1685+40C>G	NP_001029031.1:n.1685+40C>G
NM_001270447.2:c.1820+40C>G	NP_001257376.1:n.1820+40C>G
NM_001270448.2:c.1523+40C>G	NP_001257377.1:n.1523+40C>G