Canonical Allele Identifier: CA2576148093

Gene: ACADVL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7224102G>C , CM000679.2:g.7224102G>C	GRCh38
NC_000017.10:g.7127421G>C , CM000679.1:g.7127421G>C	GRCh37
NC_000017.9:g.7068145G>C	NCBI36
NG_007975.1:g.9269G>C
NG_008391.2:g.949C>G
NG_033038.1:g.15443C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1434+33G>C MANE Select	ENSP00000349297.5:n.1434+33G>C
ENST00000322910.9:c.*1389+33G>C	ENSP00000325395.5:n.*1389+33G>C
ENST00000350303.9:c.1368+33G>C	ENSP00000344152.5:n.1368+33G>C
ENST00000356839.9:c.1434+33G>C	ENSP00000349297.5:n.1434+33G>C
ENST00000542255.6:c.292+33G>C
ENST00000543245.6:c.1503+33G>C	ENSP00000438689.2:n.1503+33G>C
ENST00000578711.1:n.598G>C
ENST00000579425.5:n.550+33G>C
ENST00000579546.1:c.271+33G>C
ENST00000579894.5:n.178G>C
ENST00000583074.5:n.153+33G>C
ENST00000583850.5:n.209+33G>C
ENST00000583858.5:c.463+33G>C
ENST00000585203.6:n.625+33G>C
NM_000018.3:c.1434+33G>C	NP_000009.1:n.1434+33G>C
NM_001033859.2:c.1368+33G>C	NP_001029031.1:n.1368+33G>C
NM_001270447.1:c.1503+33G>C	NP_001257376.1:n.1503+33G>C
NM_001270448.1:c.1206+33G>C	NP_001257377.1:n.1206+33G>C
XM_006721516.2:c.1434+33G>C	XP_006721579.2:n.1434+33G>C
XM_011523829.1:c.1434+33G>C	XP_011522131.1:n.1434+33G>C
XM_011523830.1:c.1434+33G>C	XP_011522132.1:n.1434+33G>C
XR_934021.1:n.1541+33G>C
XR_934022.1:n.1541+33G>C
XR_934023.1:n.1541+33G>C
XM_006721516.3:c.1434+33G>C	XP_006721579.2:n.1434+33G>C
XM_011523829.2:c.1434+33G>C	XP_011522131.1:n.1434+33G>C
XM_011523830.2:c.1434+33G>C	XP_011522132.1:n.1434+33G>C
XM_024450741.1:c.1434+33G>C	XP_024306509.1:n.1434+33G>C
XR_934021.2:n.1493+33G>C
XR_934022.2:n.1493+33G>C
XR_934023.2:n.1493+33G>C
NM_000018.4:c.1434+33G>C MANE Select	NP_000009.1:n.1434+33G>C
NM_001033859.3:c.1368+33G>C	NP_001029031.1:n.1368+33G>C
NM_001270447.2:c.1503+33G>C	NP_001257376.1:n.1503+33G>C
NM_001270448.2:c.1206+33G>C	NP_001257377.1:n.1206+33G>C