Canonical Allele Identifier: CA2635785877

Gene: ACADVL

Linked Data

• gnomAD v4: 17-7224618-A-ACC

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7224622_7224623dup , CM000679.2:g.7224622_7224623dup	GRCh38
NC_000017.10:g.7127941_7127942dup , CM000679.1:g.7127941_7127942dup	GRCh37
NC_000017.9:g.7068665_7068666dup	NCBI36
NG_007975.1:g.9789_9790dup
NG_008391.2:g.431_432dup
NG_033038.1:g.14925_14926dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1679-20_1679-19dup MANE Select	ENSP00000349297.5:n.1679-20_1679-19dup
ENST00000322910.9:c.*1634-20_*1634-19dup	ENSP00000325395.5:n.*1634-20_*1634-19dup
ENST00000350303.9:c.1613-20_1613-19dup	ENSP00000344152.5:n.1613-20_1613-19dup
ENST00000356839.9:c.1679-20_1679-19dup	ENSP00000349297.5:n.1679-20_1679-19dup
ENST00000542255.6:c.536+70_536+71dup
ENST00000543245.6:c.1748-20_1748-19dup	ENSP00000438689.2:n.1748-20_1748-19dup
ENST00000578319.5:n.260-20_260-19dup
ENST00000578711.1:n.1118_1119dup
ENST00000578809.5:n.251-20_251-19dup
ENST00000579425.5:n.795-20_795-19dup
ENST00000579546.1:c.414-20_414-19dup
ENST00000582450.1:n.256_257dup
ENST00000583074.5:n.299+70_299+71dup
ENST00000583848.5:c.65-40_65-39dup	ENSP00000466487.1:n.65-40_65-39dup
ENST00000583850.5:n.450-20_450-19dup
ENST00000583858.5:c.610-20_610-19dup
ENST00000585203.6:n.870-20_870-19dup
NM_000018.3:c.1679-20_1679-19dup	NP_000009.1:n.1679-20_1679-19dup
NM_001033859.2:c.1613-20_1613-19dup	NP_001029031.1:n.1613-20_1613-19dup
NM_001270447.1:c.1748-20_1748-19dup	NP_001257376.1:n.1748-20_1748-19dup
NM_001270448.1:c.1451-20_1451-19dup	NP_001257377.1:n.1451-20_1451-19dup
XM_006721516.2:c.1678+70_1678+71dup	XP_006721579.2:n.1678+70_1678+71dup
XM_011523829.1:c.1576+70_1576+71dup	XP_011522131.1:n.1576+70_1576+71dup
XM_011523830.1:c.1577-20_1577-19dup	XP_011522132.1:n.1577-20_1577-19dup
XR_934021.1:n.1782-20_1782-19dup
XR_934022.1:n.1688-20_1688-19dup
XR_934023.1:n.1687+70_1687+71dup
XM_006721516.3:c.1678+70_1678+71dup	XP_006721579.2:n.1678+70_1678+71dup
XM_011523829.2:c.1576+70_1576+71dup	XP_011522131.1:n.1576+70_1576+71dup
XM_011523830.2:c.1577-20_1577-19dup	XP_011522132.1:n.1577-20_1577-19dup
XM_024450741.1:c.1667-20_1667-19dup	XP_024306509.1:n.1667-20_1667-19dup
XR_934021.2:n.1734-20_1734-19dup
XR_934022.2:n.1640-20_1640-19dup
XR_934023.2:n.1639+70_1639+71dup
NM_000018.4:c.1679-20_1679-19dup MANE Select	NP_000009.1:n.1679-20_1679-19dup
NM_001033859.3:c.1613-20_1613-19dup	NP_001029031.1:n.1613-20_1613-19dup
NM_001270447.2:c.1748-20_1748-19dup	NP_001257376.1:n.1748-20_1748-19dup
NM_001270448.2:c.1451-20_1451-19dup	NP_001257377.1:n.1451-20_1451-19dup