Canonical Allele Identifier: CA2808367582

Gene: ACADVL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7224631_7224632insCCCCCCCCA , CM000679.2:g.7224631_7224632insCCCCCCCCA	GRCh38
NC_000017.10:g.7127950_7127951insCCCCCCCCA , CM000679.1:g.7127950_7127951insCCCCCCCCA	GRCh37
NC_000017.9:g.7068674_7068675insCCCCCCCCA	NCBI36
NG_007975.1:g.9798_9799insCCCCCCCCA
NG_008391.2:g.419_420insTGGGGGGGG
NG_033038.1:g.14913_14914insTGGGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1679-11_1679-10insCCCCCCCCA MANE Select	ENSP00000349297.5:n.1679-11_1679-10insCCCCCCCCA
ENST00000322910.9:c.*1634-11_*1634-10insCCCCCCCCA	ENSP00000325395.5:n.*1634-11_*1634-10insCCCCCCCCA
ENST00000350303.9:c.1613-11_1613-10insCCCCCCCCA	ENSP00000344152.5:n.1613-11_1613-10insCCCCCCCCA
ENST00000356839.9:c.1679-11_1679-10insCCCCCCCCA	ENSP00000349297.5:n.1679-11_1679-10insCCCCCCCCA
ENST00000542255.6:c.536+79_536+80insCCCCCCCCA
ENST00000543245.6:c.1748-11_1748-10insCCCCCCCCA	ENSP00000438689.2:n.1748-11_1748-10insCCCCCCCCA
ENST00000578319.5:n.260-11_260-10insCCCCCCCCA
ENST00000578711.1:n.1127_1128insCCCCCCCCA
ENST00000578809.5:n.251-11_251-10insCCCCCCCCA
ENST00000579425.5:n.795-11_795-10insCCCCCCCCA
ENST00000579546.1:c.414-11_414-10insCCCCCCCCA
ENST00000582450.1:n.265_266insCCCCCCCCA
ENST00000583074.5:n.299+79_299+80insCCCCCCCCA
ENST00000583848.5:c.65-31_65-30insCCCCCCCCA	ENSP00000466487.1:n.65-31_65-30insCCCCCCCCA
ENST00000583850.5:n.450-11_450-10insCCCCCCCCA
ENST00000583858.5:c.610-11_610-10insCCCCCCCCA
ENST00000585203.6:n.870-11_870-10insCCCCCCCCA
NM_000018.3:c.1679-11_1679-10insCCCCCCCCA	NP_000009.1:n.1679-11_1679-10insCCCCCCCCA
NM_001033859.2:c.1613-11_1613-10insCCCCCCCCA	NP_001029031.1:n.1613-11_1613-10insCCCCCCCCA
NM_001270447.1:c.1748-11_1748-10insCCCCCCCCA	NP_001257376.1:n.1748-11_1748-10insCCCCCCCCA
NM_001270448.1:c.1451-11_1451-10insCCCCCCCCA	NP_001257377.1:n.1451-11_1451-10insCCCCCCCCA
XM_006721516.2:c.1678+79_1678+80insCCCCCCCCA	XP_006721579.2:n.1678+79_1678+80insCCCCCCCCA
XM_011523829.1:c.1576+79_1576+80insCCCCCCCCA	XP_011522131.1:n.1576+79_1576+80insCCCCCCCCA
XM_011523830.1:c.1577-11_1577-10insCCCCCCCCA	XP_011522132.1:n.1577-11_1577-10insCCCCCCCCA
XR_934021.1:n.1782-11_1782-10insCCCCCCCCA
XR_934022.1:n.1688-11_1688-10insCCCCCCCCA
XR_934023.1:n.1687+79_1687+80insCCCCCCCCA
XM_006721516.3:c.1678+79_1678+80insCCCCCCCCA	XP_006721579.2:n.1678+79_1678+80insCCCCCCCCA
XM_011523829.2:c.1576+79_1576+80insCCCCCCCCA	XP_011522131.1:n.1576+79_1576+80insCCCCCCCCA
XM_011523830.2:c.1577-11_1577-10insCCCCCCCCA	XP_011522132.1:n.1577-11_1577-10insCCCCCCCCA
XM_024450741.1:c.1667-11_1667-10insCCCCCCCCA	XP_024306509.1:n.1667-11_1667-10insCCCCCCCCA
XR_934021.2:n.1734-11_1734-10insCCCCCCCCA
XR_934022.2:n.1640-11_1640-10insCCCCCCCCA
XR_934023.2:n.1639+79_1639+80insCCCCCCCCA
NM_000018.4:c.1679-11_1679-10insCCCCCCCCA MANE Select	NP_000009.1:n.1679-11_1679-10insCCCCCCCCA
NM_001033859.3:c.1613-11_1613-10insCCCCCCCCA	NP_001029031.1:n.1613-11_1613-10insCCCCCCCCA
NM_001270447.2:c.1748-11_1748-10insCCCCCCCCA	NP_001257376.1:n.1748-11_1748-10insCCCCCCCCA
NM_001270448.2:c.1451-11_1451-10insCCCCCCCCA	NP_001257377.1:n.1451-11_1451-10insCCCCCCCCA