Canonical Allele Identifier: CA2838752709

Gene: ACADVL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7223897A>G , CM000679.2:g.7223897A>G	GRCh38
NC_000017.10:g.7127216A>G , CM000679.1:g.7127216A>G	GRCh37
NC_000017.9:g.7067940A>G	NCBI36
NG_007975.1:g.9064A>G
NG_008391.2:g.1154T>C
NG_033038.1:g.15648T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1332+22A>G MANE Select	ENSP00000349297.5:n.1332+22A>G
ENST00000322910.9:c.*1287+22A>G	ENSP00000325395.5:n.*1287+22A>G
ENST00000350303.9:c.1266+22A>G	ENSP00000344152.5:n.1266+22A>G
ENST00000356839.9:c.1332+22A>G	ENSP00000349297.5:n.1332+22A>G
ENST00000542255.6:c.190+22A>G
ENST00000543245.6:c.1401+22A>G	ENSP00000438689.2:n.1401+22A>G
ENST00000578711.1:n.393A>G
ENST00000579425.5:n.378A>G
ENST00000579546.1:c.169+22A>G
ENST00000583074.5:n.51+22A>G
ENST00000583850.5:n.107+22A>G
ENST00000583858.5:c.361+22A>G
ENST00000585203.6:n.523+39A>G
NM_000018.3:c.1332+22A>G	NP_000009.1:n.1332+22A>G
NM_001033859.2:c.1266+22A>G	NP_001029031.1:n.1266+22A>G
NM_001270447.1:c.1401+22A>G	NP_001257376.1:n.1401+22A>G
NM_001270448.1:c.1104+22A>G	NP_001257377.1:n.1104+22A>G
XM_006721516.2:c.1332+22A>G	XP_006721579.2:n.1332+22A>G
XM_011523829.1:c.1332+22A>G	XP_011522131.1:n.1332+22A>G
XM_011523830.1:c.1332+22A>G	XP_011522132.1:n.1332+22A>G
XR_934021.1:n.1439+22A>G
XR_934022.1:n.1439+22A>G
XR_934023.1:n.1439+22A>G
XM_006721516.3:c.1332+22A>G	XP_006721579.2:n.1332+22A>G
XM_011523829.2:c.1332+22A>G	XP_011522131.1:n.1332+22A>G
XM_011523830.2:c.1332+22A>G	XP_011522132.1:n.1332+22A>G
XM_024450741.1:c.1332+22A>G	XP_024306509.1:n.1332+22A>G
XR_934021.2:n.1391+22A>G
XR_934022.2:n.1391+22A>G
XR_934023.2:n.1391+22A>G
NM_000018.4:c.1332+22A>G MANE Select	NP_000009.1:n.1332+22A>G
NM_001033859.3:c.1266+22A>G	NP_001029031.1:n.1266+22A>G
NM_001270447.2:c.1401+22A>G	NP_001257376.1:n.1401+22A>G
NM_001270448.2:c.1104+22A>G	NP_001257377.1:n.1104+22A>G