Canonical Allele Identifier: CA2635785667

Gene: ACADVL

Linked Data

• gnomAD v4: 17-7224612-A-ACCCACCCCCCCCCCCCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7224615_7224616insACCCCCCCCCCCCCCCCC , CM000679.2:g.7224615_7224616insACCCCCCCCCCCCCCCCC	GRCh38
NC_000017.10:g.7127934_7127935insACCCCCCCCCCCCCCCCC , CM000679.1:g.7127934_7127935insACCCCCCCCCCCCCCCCC	GRCh37
NC_000017.9:g.7068658_7068659insACCCCCCCCCCCCCCCCC	NCBI36
NG_007975.1:g.9782_9783insACCCCCCCCCCCCCCCCC
NG_008391.2:g.438_439insGGGGGGGGGGGGGGTGGG
NG_033038.1:g.14932_14933insGGGGGGGGGGGGGGTGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1679-27_1679-26insACCCCCCCCCCCCCCCCC MANE Select	ENSP00000349297.5:n.1679-27_1679-26insACCCCCCCCCCCCCCCCC
ENST00000322910.9:c.*1634-27_*1634-26insACCCCCCCCCCCCCCCCC	ENSP00000325395.5:n.*1634-27_*1634-26insACCCCCCCCCCCCCCCCC
ENST00000350303.9:c.1613-27_1613-26insACCCCCCCCCCCCCCCCC	ENSP00000344152.5:n.1613-27_1613-26insACCCCCCCCCCCCCCCCC
ENST00000356839.9:c.1679-27_1679-26insACCCCCCCCCCCCCCCCC	ENSP00000349297.5:n.1679-27_1679-26insACCCCCCCCCCCCCCCCC
ENST00000542255.6:c.536+63_536+64insACCCCCCCCCCCCCCCCC
ENST00000543245.6:c.1748-27_1748-26insACCCCCCCCCCCCCCCCC	ENSP00000438689.2:n.1748-27_1748-26insACCCCCCCCCCCCCCCCC
ENST00000578319.5:n.260-27_260-26insACCCCCCCCCCCCCCCCC
ENST00000578711.1:n.1111_1112insACCCCCCCCCCCCCCCCC
ENST00000578809.5:n.251-27_251-26insACCCCCCCCCCCCCCCCC
ENST00000579425.5:n.795-27_795-26insACCCCCCCCCCCCCCCCC
ENST00000579546.1:c.414-27_414-26insACCCCCCCCCCCCCCCCC
ENST00000582450.1:n.249_250insACCCCCCCCCCCCCCCCC
ENST00000583074.5:n.299+63_299+64insACCCCCCCCCCCCCCCCC
ENST00000583848.5:c.65-47_65-46insACCCCCCCCCCCCCCCCC	ENSP00000466487.1:n.65-47_65-46insACCCCCCCCCCCCCCCCC
ENST00000583850.5:n.450-27_450-26insACCCCCCCCCCCCCCCCC
ENST00000583858.5:c.610-27_610-26insACCCCCCCCCCCCCCCCC
ENST00000585203.6:n.870-27_870-26insACCCCCCCCCCCCCCCCC
NM_000018.3:c.1679-27_1679-26insACCCCCCCCCCCCCCCCC	NP_000009.1:n.1679-27_1679-26insACCCCCCCCCCCCCCCCC
NM_001033859.2:c.1613-27_1613-26insACCCCCCCCCCCCCCCCC	NP_001029031.1:n.1613-27_1613-26insACCCCCCCCCCCCCCCCC
NM_001270447.1:c.1748-27_1748-26insACCCCCCCCCCCCCCCCC	NP_001257376.1:n.1748-27_1748-26insACCCCCCCCCCCCCCCCC
NM_001270448.1:c.1451-27_1451-26insACCCCCCCCCCCCCCCCC	NP_001257377.1:n.1451-27_1451-26insACCCCCCCCCCCCCCCCC
XM_006721516.2:c.1678+63_1678+64insACCCCCCCCCCCCCCCCC	XP_006721579.2:n.1678+63_1678+64insACCCCCCCCCCCCCCCCC
XM_011523829.1:c.1576+63_1576+64insACCCCCCCCCCCCCCCCC	XP_011522131.1:n.1576+63_1576+64insACCCCCCCCCCCCCCCCC
XM_011523830.1:c.1577-27_1577-26insACCCCCCCCCCCCCCCCC	XP_011522132.1:n.1577-27_1577-26insACCCCCCCCCCCCCCCCC
XR_934021.1:n.1782-27_1782-26insACCCCCCCCCCCCCCCCC
XR_934022.1:n.1688-27_1688-26insACCCCCCCCCCCCCCCCC
XR_934023.1:n.1687+63_1687+64insACCCCCCCCCCCCCCCCC
XM_006721516.3:c.1678+63_1678+64insACCCCCCCCCCCCCCCCC	XP_006721579.2:n.1678+63_1678+64insACCCCCCCCCCCCCCCCC
XM_011523829.2:c.1576+63_1576+64insACCCCCCCCCCCCCCCCC	XP_011522131.1:n.1576+63_1576+64insACCCCCCCCCCCCCCCCC
XM_011523830.2:c.1577-27_1577-26insACCCCCCCCCCCCCCCCC	XP_011522132.1:n.1577-27_1577-26insACCCCCCCCCCCCCCCCC
XM_024450741.1:c.1667-27_1667-26insACCCCCCCCCCCCCCCCC	XP_024306509.1:n.1667-27_1667-26insACCCCCCCCCCCCCCCCC
XR_934021.2:n.1734-27_1734-26insACCCCCCCCCCCCCCCCC
XR_934022.2:n.1640-27_1640-26insACCCCCCCCCCCCCCCCC
XR_934023.2:n.1639+63_1639+64insACCCCCCCCCCCCCCCCC
NM_000018.4:c.1679-27_1679-26insACCCCCCCCCCCCCCCCC MANE Select	NP_000009.1:n.1679-27_1679-26insACCCCCCCCCCCCCCCCC
NM_001033859.3:c.1613-27_1613-26insACCCCCCCCCCCCCCCCC	NP_001029031.1:n.1613-27_1613-26insACCCCCCCCCCCCCCCCC
NM_001270447.2:c.1748-27_1748-26insACCCCCCCCCCCCCCCCC	NP_001257376.1:n.1748-27_1748-26insACCCCCCCCCCCCCCCCC
NM_001270448.2:c.1451-27_1451-26insACCCCCCCCCCCCCCCCC	NP_001257377.1:n.1451-27_1451-26insACCCCCCCCCCCCCCCCC