Canonical Allele Identifier: CA981155057

Gene: ACADVL

Linked Data

• gnomAD v3: 17-7224612-A-ACCCCCCCCCCC
• gnomAD v4: 17-7224612-A-ACCCCCCCCCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7224617_7224618insCCCCCCCCCCC , CM000679.2:g.7224617_7224618insCCCCCCCCCCC	GRCh38
NC_000017.10:g.7127936_7127937insCCCCCCCCCCC , CM000679.1:g.7127936_7127937insCCCCCCCCCCC	GRCh37
NC_000017.9:g.7068660_7068661insCCCCCCCCCCC	NCBI36
NG_007975.1:g.9784_9785insCCCCCCCCCCC
NG_008391.2:g.438_439insGGGGGGGGGGG
NG_033038.1:g.14932_14933insGGGGGGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1679-25_1679-24insCCCCCCCCCCC MANE Select	ENSP00000349297.5:n.1679-25_1679-24insCCCCCCCCCCC
ENST00000322910.9:c.*1634-25_*1634-24insCCCCCCCCCCC	ENSP00000325395.5:n.*1634-25_*1634-24insCCCCCCCCCCC
ENST00000350303.9:c.1613-25_1613-24insCCCCCCCCCCC	ENSP00000344152.5:n.1613-25_1613-24insCCCCCCCCCCC
ENST00000356839.9:c.1679-25_1679-24insCCCCCCCCCCC	ENSP00000349297.5:n.1679-25_1679-24insCCCCCCCCCCC
ENST00000542255.6:c.536+65_536+66insCCCCCCCCCCC
ENST00000543245.6:c.1748-25_1748-24insCCCCCCCCCCC	ENSP00000438689.2:n.1748-25_1748-24insCCCCCCCCCCC
ENST00000578319.5:n.260-25_260-24insCCCCCCCCCCC
ENST00000578711.1:n.1113_1114insCCCCCCCCCCC
ENST00000578809.5:n.251-25_251-24insCCCCCCCCCCC
ENST00000579425.5:n.795-25_795-24insCCCCCCCCCCC
ENST00000579546.1:c.414-25_414-24insCCCCCCCCCCC
ENST00000582450.1:n.251_252insCCCCCCCCCCC
ENST00000583074.5:n.299+65_299+66insCCCCCCCCCCC
ENST00000583848.5:c.65-45_65-44insCCCCCCCCCCC	ENSP00000466487.1:n.65-45_65-44insCCCCCCCCCCC
ENST00000583850.5:n.450-25_450-24insCCCCCCCCCCC
ENST00000583858.5:c.610-25_610-24insCCCCCCCCCCC
ENST00000585203.6:n.870-25_870-24insCCCCCCCCCCC
NM_000018.3:c.1679-25_1679-24insCCCCCCCCCCC	NP_000009.1:n.1679-25_1679-24insCCCCCCCCCCC
NM_001033859.2:c.1613-25_1613-24insCCCCCCCCCCC	NP_001029031.1:n.1613-25_1613-24insCCCCCCCCCCC
NM_001270447.1:c.1748-25_1748-24insCCCCCCCCCCC	NP_001257376.1:n.1748-25_1748-24insCCCCCCCCCCC
NM_001270448.1:c.1451-25_1451-24insCCCCCCCCCCC	NP_001257377.1:n.1451-25_1451-24insCCCCCCCCCCC
XM_006721516.2:c.1678+65_1678+66insCCCCCCCCCCC	XP_006721579.2:n.1678+65_1678+66insCCCCCCCCCCC
XM_011523829.1:c.1576+65_1576+66insCCCCCCCCCCC	XP_011522131.1:n.1576+65_1576+66insCCCCCCCCCCC
XM_011523830.1:c.1577-25_1577-24insCCCCCCCCCCC	XP_011522132.1:n.1577-25_1577-24insCCCCCCCCCCC
XR_934021.1:n.1782-25_1782-24insCCCCCCCCCCC
XR_934022.1:n.1688-25_1688-24insCCCCCCCCCCC
XR_934023.1:n.1687+65_1687+66insCCCCCCCCCCC
XM_006721516.3:c.1678+65_1678+66insCCCCCCCCCCC	XP_006721579.2:n.1678+65_1678+66insCCCCCCCCCCC
XM_011523829.2:c.1576+65_1576+66insCCCCCCCCCCC	XP_011522131.1:n.1576+65_1576+66insCCCCCCCCCCC
XM_011523830.2:c.1577-25_1577-24insCCCCCCCCCCC	XP_011522132.1:n.1577-25_1577-24insCCCCCCCCCCC
XM_024450741.1:c.1667-25_1667-24insCCCCCCCCCCC	XP_024306509.1:n.1667-25_1667-24insCCCCCCCCCCC
XR_934021.2:n.1734-25_1734-24insCCCCCCCCCCC
XR_934022.2:n.1640-25_1640-24insCCCCCCCCCCC
XR_934023.2:n.1639+65_1639+66insCCCCCCCCCCC
NM_000018.4:c.1679-25_1679-24insCCCCCCCCCCC MANE Select	NP_000009.1:n.1679-25_1679-24insCCCCCCCCCCC
NM_001033859.3:c.1613-25_1613-24insCCCCCCCCCCC	NP_001029031.1:n.1613-25_1613-24insCCCCCCCCCCC
NM_001270447.2:c.1748-25_1748-24insCCCCCCCCCCC	NP_001257376.1:n.1748-25_1748-24insCCCCCCCCCCC
NM_001270448.2:c.1451-25_1451-24insCCCCCCCCCCC	NP_001257377.1:n.1451-25_1451-24insCCCCCCCCCCC