Canonical Allele Identifier: CA2635785159

Gene: ACADVL

Linked Data

• gnomAD v4: 17-7224606-G-GCCCCTCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7224610_7224611insTCCCCCCC , CM000679.2:g.7224610_7224611insTCCCCCCC	GRCh38
NC_000017.10:g.7127929_7127930insTCCCCCCC , CM000679.1:g.7127929_7127930insTCCCCCCC	GRCh37
NC_000017.9:g.7068653_7068654insTCCCCCCC	NCBI36
NG_007975.1:g.9777_9778insTCCCCCCC
NG_008391.2:g.444_445insGGGAGGGG
NG_033038.1:g.14938_14939insGGGAGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1679-32_1679-31insTCCCCCCC MANE Select	ENSP00000349297.5:n.1679-32_1679-31insTCCCCCCC
ENST00000322910.9:c.*1634-32_*1634-31insTCCCCCCC	ENSP00000325395.5:n.*1634-32_*1634-31insTCCCCCCC
ENST00000350303.9:c.1613-32_1613-31insTCCCCCCC	ENSP00000344152.5:n.1613-32_1613-31insTCCCCCCC
ENST00000356839.9:c.1679-32_1679-31insTCCCCCCC	ENSP00000349297.5:n.1679-32_1679-31insTCCCCCCC
ENST00000542255.6:c.536+58_536+59insTCCCCCCC
ENST00000543245.6:c.1748-32_1748-31insTCCCCCCC	ENSP00000438689.2:n.1748-32_1748-31insTCCCCCCC
ENST00000578319.5:n.260-32_260-31insTCCCCCCC
ENST00000578711.1:n.1106_1107insTCCCCCCC
ENST00000578809.5:n.251-32_251-31insTCCCCCCC
ENST00000579391.1:n.340_341insTCCCCCCC
ENST00000579425.5:n.795-32_795-31insTCCCCCCC
ENST00000579546.1:c.414-32_414-31insTCCCCCCC
ENST00000582450.1:n.244_245insTCCCCCCC
ENST00000583074.5:n.299+58_299+59insTCCCCCCC
ENST00000583848.5:c.65-52_65-51insTCCCCCCC	ENSP00000466487.1:n.65-52_65-51insTCCCCCCC
ENST00000583850.5:n.450-32_450-31insTCCCCCCC
ENST00000583858.5:c.610-32_610-31insTCCCCCCC
ENST00000585203.6:n.870-32_870-31insTCCCCCCC
NM_000018.3:c.1679-32_1679-31insTCCCCCCC	NP_000009.1:n.1679-32_1679-31insTCCCCCCC
NM_001033859.2:c.1613-32_1613-31insTCCCCCCC	NP_001029031.1:n.1613-32_1613-31insTCCCCCCC
NM_001270447.1:c.1748-32_1748-31insTCCCCCCC	NP_001257376.1:n.1748-32_1748-31insTCCCCCCC
NM_001270448.1:c.1451-32_1451-31insTCCCCCCC	NP_001257377.1:n.1451-32_1451-31insTCCCCCCC
XM_006721516.2:c.1678+58_1678+59insTCCCCCCC	XP_006721579.2:n.1678+58_1678+59insTCCCCCCC
XM_011523829.1:c.1576+58_1576+59insTCCCCCCC	XP_011522131.1:n.1576+58_1576+59insTCCCCCCC
XM_011523830.1:c.1577-32_1577-31insTCCCCCCC	XP_011522132.1:n.1577-32_1577-31insTCCCCCCC
XR_934021.1:n.1782-32_1782-31insTCCCCCCC
XR_934022.1:n.1688-32_1688-31insTCCCCCCC
XR_934023.1:n.1687+58_1687+59insTCCCCCCC
XM_006721516.3:c.1678+58_1678+59insTCCCCCCC	XP_006721579.2:n.1678+58_1678+59insTCCCCCCC
XM_011523829.2:c.1576+58_1576+59insTCCCCCCC	XP_011522131.1:n.1576+58_1576+59insTCCCCCCC
XM_011523830.2:c.1577-32_1577-31insTCCCCCCC	XP_011522132.1:n.1577-32_1577-31insTCCCCCCC
XM_024450741.1:c.1667-32_1667-31insTCCCCCCC	XP_024306509.1:n.1667-32_1667-31insTCCCCCCC
XR_934021.2:n.1734-32_1734-31insTCCCCCCC
XR_934022.2:n.1640-32_1640-31insTCCCCCCC
XR_934023.2:n.1639+58_1639+59insTCCCCCCC
NM_000018.4:c.1679-32_1679-31insTCCCCCCC MANE Select	NP_000009.1:n.1679-32_1679-31insTCCCCCCC
NM_001033859.3:c.1613-32_1613-31insTCCCCCCC	NP_001029031.1:n.1613-32_1613-31insTCCCCCCC
NM_001270447.2:c.1748-32_1748-31insTCCCCCCC	NP_001257376.1:n.1748-32_1748-31insTCCCCCCC
NM_001270448.2:c.1451-32_1451-31insTCCCCCCC	NP_001257377.1:n.1451-32_1451-31insTCCCCCCC