Canonical Allele Identifier: CA2635785313

Gene: ACADVL

Linked Data

• gnomAD v4: 17-7224607-C-CCG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7224608_7224609insGC , CM000679.2:g.7224608_7224609insGC	GRCh38
NC_000017.10:g.7127927_7127928insGC , CM000679.1:g.7127927_7127928insGC	GRCh37
NC_000017.9:g.7068651_7068652insGC	NCBI36
NG_007975.1:g.9775_9776insGC
NG_008391.2:g.443_444insCG
NG_033038.1:g.14937_14938insCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1679-34_1679-33insGC MANE Select	ENSP00000349297.5:n.1679-34_1679-33insGC
ENST00000322910.9:c.*1634-34_*1634-33insGC	ENSP00000325395.5:n.*1634-34_*1634-33insGC
ENST00000350303.9:c.1613-34_1613-33insGC	ENSP00000344152.5:n.1613-34_1613-33insGC
ENST00000356839.9:c.1679-34_1679-33insGC	ENSP00000349297.5:n.1679-34_1679-33insGC
ENST00000542255.6:c.536+56_536+57insGC
ENST00000543245.6:c.1748-34_1748-33insGC	ENSP00000438689.2:n.1748-34_1748-33insGC
ENST00000578319.5:n.260-34_260-33insGC
ENST00000578711.1:n.1104_1105insGC
ENST00000578809.5:n.251-34_251-33insGC
ENST00000579391.1:n.338_339insGC
ENST00000579425.5:n.795-34_795-33insGC
ENST00000579546.1:c.414-34_414-33insGC
ENST00000582450.1:n.242_243insGC
ENST00000583074.5:n.299+56_299+57insGC
ENST00000583848.5:c.65-54_65-53insGC	ENSP00000466487.1:n.65-54_65-53insGC
ENST00000583850.5:n.450-34_450-33insGC
ENST00000583858.5:c.610-34_610-33insGC
ENST00000585203.6:n.870-34_870-33insGC
NM_000018.3:c.1679-34_1679-33insGC	NP_000009.1:n.1679-34_1679-33insGC
NM_001033859.2:c.1613-34_1613-33insGC	NP_001029031.1:n.1613-34_1613-33insGC
NM_001270447.1:c.1748-34_1748-33insGC	NP_001257376.1:n.1748-34_1748-33insGC
NM_001270448.1:c.1451-34_1451-33insGC	NP_001257377.1:n.1451-34_1451-33insGC
XM_006721516.2:c.1678+56_1678+57insGC	XP_006721579.2:n.1678+56_1678+57insGC
XM_011523829.1:c.1576+56_1576+57insGC	XP_011522131.1:n.1576+56_1576+57insGC
XM_011523830.1:c.1577-34_1577-33insGC	XP_011522132.1:n.1577-34_1577-33insGC
XR_934021.1:n.1782-34_1782-33insGC
XR_934022.1:n.1688-34_1688-33insGC
XR_934023.1:n.1687+56_1687+57insGC
XM_006721516.3:c.1678+56_1678+57insGC	XP_006721579.2:n.1678+56_1678+57insGC
XM_011523829.2:c.1576+56_1576+57insGC	XP_011522131.1:n.1576+56_1576+57insGC
XM_011523830.2:c.1577-34_1577-33insGC	XP_011522132.1:n.1577-34_1577-33insGC
XM_024450741.1:c.1667-34_1667-33insGC	XP_024306509.1:n.1667-34_1667-33insGC
XR_934021.2:n.1734-34_1734-33insGC
XR_934022.2:n.1640-34_1640-33insGC
XR_934023.2:n.1639+56_1639+57insGC
NM_000018.4:c.1679-34_1679-33insGC MANE Select	NP_000009.1:n.1679-34_1679-33insGC
NM_001033859.3:c.1613-34_1613-33insGC	NP_001029031.1:n.1613-34_1613-33insGC
NM_001270447.2:c.1748-34_1748-33insGC	NP_001257376.1:n.1748-34_1748-33insGC
NM_001270448.2:c.1451-34_1451-33insGC	NP_001257377.1:n.1451-34_1451-33insGC