Canonical Allele Identifier: CA2635785759

Gene: ACADVL

Linked Data

• gnomAD v4: 17-7224614-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7224614_7224615insA , CM000679.2:g.7224614_7224615insA	GRCh38
NC_000017.10:g.7127933_7127934insA , CM000679.1:g.7127933_7127934insA	GRCh37
NC_000017.9:g.7068657_7068658insA	NCBI36
NG_007975.1:g.9781_9782insA
NG_008391.2:g.436_437insT
NG_033038.1:g.14930_14931insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1679-28_1679-27insA MANE Select	ENSP00000349297.5:n.1679-28_1679-27insA
ENST00000322910.9:c.*1634-28_*1634-27insA	ENSP00000325395.5:n.*1634-28_*1634-27insA
ENST00000350303.9:c.1613-28_1613-27insA	ENSP00000344152.5:n.1613-28_1613-27insA
ENST00000356839.9:c.1679-28_1679-27insA	ENSP00000349297.5:n.1679-28_1679-27insA
ENST00000542255.6:c.536+62_536+63insA
ENST00000543245.6:c.1748-28_1748-27insA	ENSP00000438689.2:n.1748-28_1748-27insA
ENST00000578319.5:n.260-28_260-27insA
ENST00000578711.1:n.1110_1111insA
ENST00000578809.5:n.251-28_251-27insA
ENST00000579425.5:n.795-28_795-27insA
ENST00000579546.1:c.414-28_414-27insA
ENST00000582450.1:n.248_249insA
ENST00000583074.5:n.299+62_299+63insA
ENST00000583848.5:c.65-48_65-47insA	ENSP00000466487.1:n.65-48_65-47insA
ENST00000583850.5:n.450-28_450-27insA
ENST00000583858.5:c.610-28_610-27insA
ENST00000585203.6:n.870-28_870-27insA
NM_000018.3:c.1679-28_1679-27insA	NP_000009.1:n.1679-28_1679-27insA
NM_001033859.2:c.1613-28_1613-27insA	NP_001029031.1:n.1613-28_1613-27insA
NM_001270447.1:c.1748-28_1748-27insA	NP_001257376.1:n.1748-28_1748-27insA
NM_001270448.1:c.1451-28_1451-27insA	NP_001257377.1:n.1451-28_1451-27insA
XM_006721516.2:c.1678+62_1678+63insA	XP_006721579.2:n.1678+62_1678+63insA
XM_011523829.1:c.1576+62_1576+63insA	XP_011522131.1:n.1576+62_1576+63insA
XM_011523830.1:c.1577-28_1577-27insA	XP_011522132.1:n.1577-28_1577-27insA
XR_934021.1:n.1782-28_1782-27insA
XR_934022.1:n.1688-28_1688-27insA
XR_934023.1:n.1687+62_1687+63insA
XM_006721516.3:c.1678+62_1678+63insA	XP_006721579.2:n.1678+62_1678+63insA
XM_011523829.2:c.1576+62_1576+63insA	XP_011522131.1:n.1576+62_1576+63insA
XM_011523830.2:c.1577-28_1577-27insA	XP_011522132.1:n.1577-28_1577-27insA
XM_024450741.1:c.1667-28_1667-27insA	XP_024306509.1:n.1667-28_1667-27insA
XR_934021.2:n.1734-28_1734-27insA
XR_934022.2:n.1640-28_1640-27insA
XR_934023.2:n.1639+62_1639+63insA
NM_000018.4:c.1679-28_1679-27insA MANE Select	NP_000009.1:n.1679-28_1679-27insA
NM_001033859.3:c.1613-28_1613-27insA	NP_001029031.1:n.1613-28_1613-27insA
NM_001270447.2:c.1748-28_1748-27insA	NP_001257376.1:n.1748-28_1748-27insA
NM_001270448.2:c.1451-28_1451-27insA	NP_001257377.1:n.1451-28_1451-27insA