Canonical Allele Identifier: CA2808367576

Gene: ACADVL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7224624_7224625insGTCCCTCCAGCAGTG , CM000679.2:g.7224624_7224625insGTCCCTCCAGCAGTG	GRCh38
NC_000017.10:g.7127943_7127944insGTCCCTCCAGCAGTG , CM000679.1:g.7127943_7127944insGTCCCTCCAGCAGTG	GRCh37
NC_000017.9:g.7068667_7068668insGTCCCTCCAGCAGTG	NCBI36
NG_007975.1:g.9791_9792insGTCCCTCCAGCAGTG
NG_008391.2:g.426_427insCACTGCTGGAGGGAC
NG_033038.1:g.14920_14921insCACTGCTGGAGGGAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1679-18_1679-17insGTCCCTCCAGCAGTG MANE Select	ENSP00000349297.5:n.1679-18_1679-17insGTCCCTCCAGCAGTG
ENST00000322910.9:c.*1634-18_*1634-17insGTCCCTCCAGCAGTG	ENSP00000325395.5:n.*1634-18_*1634-17insGTCCCTCCAGCAGTG
ENST00000350303.9:c.1613-18_1613-17insGTCCCTCCAGCAGTG	ENSP00000344152.5:n.1613-18_1613-17insGTCCCTCCAGCAGTG
ENST00000356839.9:c.1679-18_1679-17insGTCCCTCCAGCAGTG	ENSP00000349297.5:n.1679-18_1679-17insGTCCCTCCAGCAGTG
ENST00000542255.6:c.536+72_536+73insGTCCCTCCAGCAGTG
ENST00000543245.6:c.1748-18_1748-17insGTCCCTCCAGCAGTG	ENSP00000438689.2:n.1748-18_1748-17insGTCCCTCCAGCAGTG
ENST00000578319.5:n.260-18_260-17insGTCCCTCCAGCAGTG
ENST00000578711.1:n.1120_1121insGTCCCTCCAGCAGTG
ENST00000578809.5:n.251-18_251-17insGTCCCTCCAGCAGTG
ENST00000579425.5:n.795-18_795-17insGTCCCTCCAGCAGTG
ENST00000579546.1:c.414-18_414-17insGTCCCTCCAGCAGTG
ENST00000582450.1:n.258_259insGTCCCTCCAGCAGTG
ENST00000583074.5:n.299+72_299+73insGTCCCTCCAGCAGTG
ENST00000583848.5:c.65-38_65-37insGTCCCTCCAGCAGTG	ENSP00000466487.1:n.65-38_65-37insGTCCCTCCAGCAGTG
ENST00000583850.5:n.450-18_450-17insGTCCCTCCAGCAGTG
ENST00000583858.5:c.610-18_610-17insGTCCCTCCAGCAGTG
ENST00000585203.6:n.870-18_870-17insGTCCCTCCAGCAGTG
NM_000018.3:c.1679-18_1679-17insGTCCCTCCAGCAGTG	NP_000009.1:n.1679-18_1679-17insGTCCCTCCAGCAGTG
NM_001033859.2:c.1613-18_1613-17insGTCCCTCCAGCAGTG	NP_001029031.1:n.1613-18_1613-17insGTCCCTCCAGCAGTG
NM_001270447.1:c.1748-18_1748-17insGTCCCTCCAGCAGTG	NP_001257376.1:n.1748-18_1748-17insGTCCCTCCAGCAGTG
NM_001270448.1:c.1451-18_1451-17insGTCCCTCCAGCAGTG	NP_001257377.1:n.1451-18_1451-17insGTCCCTCCAGCAGTG
XM_006721516.2:c.1678+72_1678+73insGTCCCTCCAGCAGTG	XP_006721579.2:n.1678+72_1678+73insGTCCCTCCAGCAGTG
XM_011523829.1:c.1576+72_1576+73insGTCCCTCCAGCAGTG	XP_011522131.1:n.1576+72_1576+73insGTCCCTCCAGCAGTG
XM_011523830.1:c.1577-18_1577-17insGTCCCTCCAGCAGTG	XP_011522132.1:n.1577-18_1577-17insGTCCCTCCAGCAGTG
XR_934021.1:n.1782-18_1782-17insGTCCCTCCAGCAGTG
XR_934022.1:n.1688-18_1688-17insGTCCCTCCAGCAGTG
XR_934023.1:n.1687+72_1687+73insGTCCCTCCAGCAGTG
XM_006721516.3:c.1678+72_1678+73insGTCCCTCCAGCAGTG	XP_006721579.2:n.1678+72_1678+73insGTCCCTCCAGCAGTG
XM_011523829.2:c.1576+72_1576+73insGTCCCTCCAGCAGTG	XP_011522131.1:n.1576+72_1576+73insGTCCCTCCAGCAGTG
XM_011523830.2:c.1577-18_1577-17insGTCCCTCCAGCAGTG	XP_011522132.1:n.1577-18_1577-17insGTCCCTCCAGCAGTG
XM_024450741.1:c.1667-18_1667-17insGTCCCTCCAGCAGTG	XP_024306509.1:n.1667-18_1667-17insGTCCCTCCAGCAGTG
XR_934021.2:n.1734-18_1734-17insGTCCCTCCAGCAGTG
XR_934022.2:n.1640-18_1640-17insGTCCCTCCAGCAGTG
XR_934023.2:n.1639+72_1639+73insGTCCCTCCAGCAGTG
NM_000018.4:c.1679-18_1679-17insGTCCCTCCAGCAGTG MANE Select	NP_000009.1:n.1679-18_1679-17insGTCCCTCCAGCAGTG
NM_001033859.3:c.1613-18_1613-17insGTCCCTCCAGCAGTG	NP_001029031.1:n.1613-18_1613-17insGTCCCTCCAGCAGTG
NM_001270447.2:c.1748-18_1748-17insGTCCCTCCAGCAGTG	NP_001257376.1:n.1748-18_1748-17insGTCCCTCCAGCAGTG
NM_001270448.2:c.1451-18_1451-17insGTCCCTCCAGCAGTG	NP_001257377.1:n.1451-18_1451-17insGTCCCTCCAGCAGTG