Canonical Allele Identifier: CA2635786268
Gene: ACADVL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224633_7224634insAC , CM000679.2:g.7224633_7224634insAC GRCh38
NC_000017.10:g.7127952_7127953insAC , CM000679.1:g.7127952_7127953insAC GRCh37
NC_000017.9:g.7068676_7068677insAC NCBI36
NG_007975.1:g.9800_9801insAC
NG_008391.2:g.417_418insGT
NG_033038.1:g.14911_14912insGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1679-9_1679-8insAC MANE Select ENSP00000349297.5:n.1679-9_1679-8insAC
ENST00000322910.9:c.*1634-9_*1634-8insAC ENSP00000325395.5:n.*1634-9_*1634-8insAC
ENST00000350303.9:c.1613-9_1613-8insAC ENSP00000344152.5:n.1613-9_1613-8insAC
ENST00000356839.9:c.1679-9_1679-8insAC ENSP00000349297.5:n.1679-9_1679-8insAC
ENST00000542255.6:c.537-82_537-81insAC
ENST00000543245.6:c.1748-9_1748-8insAC ENSP00000438689.2:n.1748-9_1748-8insAC
ENST00000578033.1:n.1_2insAC
ENST00000578319.5:n.260-9_260-8insAC
ENST00000578711.1:n.1129_1130insAC
ENST00000578809.5:n.251-9_251-8insAC
ENST00000579425.5:n.795-9_795-8insAC
ENST00000579546.1:c.414-9_414-8insAC
ENST00000582450.1:n.267_268insAC
ENST00000583074.5:n.300-82_300-81insAC
ENST00000583848.5:c.65-29_65-28insAC ENSP00000466487.1:n.65-29_65-28insAC
ENST00000583850.5:n.450-9_450-8insAC
ENST00000583858.5:c.610-9_610-8insAC
ENST00000585203.6:n.870-9_870-8insAC
NM_000018.3:c.1679-9_1679-8insAC NP_000009.1:n.1679-9_1679-8insAC
NM_001033859.2:c.1613-9_1613-8insAC NP_001029031.1:n.1613-9_1613-8insAC
NM_001270447.1:c.1748-9_1748-8insAC NP_001257376.1:n.1748-9_1748-8insAC
NM_001270448.1:c.1451-9_1451-8insAC NP_001257377.1:n.1451-9_1451-8insAC
XM_006721516.2:c.1679-82_1679-81insAC XP_006721579.2:n.1679-82_1679-81insAC
XM_011523829.1:c.1577-82_1577-81insAC XP_011522131.1:n.1577-82_1577-81insAC
XM_011523830.1:c.1577-9_1577-8insAC XP_011522132.1:n.1577-9_1577-8insAC
XR_934021.1:n.1782-9_1782-8insAC
XR_934022.1:n.1688-9_1688-8insAC
XR_934023.1:n.1688-82_1688-81insAC
XM_006721516.3:c.1679-82_1679-81insAC XP_006721579.2:n.1679-82_1679-81insAC
XM_011523829.2:c.1577-82_1577-81insAC XP_011522131.1:n.1577-82_1577-81insAC
XM_011523830.2:c.1577-9_1577-8insAC XP_011522132.1:n.1577-9_1577-8insAC
XM_024450741.1:c.1667-9_1667-8insAC XP_024306509.1:n.1667-9_1667-8insAC
XR_934021.2:n.1734-9_1734-8insAC
XR_934022.2:n.1640-9_1640-8insAC
XR_934023.2:n.1640-82_1640-81insAC
NM_000018.4:c.1679-9_1679-8insAC MANE Select NP_000009.1:n.1679-9_1679-8insAC
NM_001033859.3:c.1613-9_1613-8insAC NP_001029031.1:n.1613-9_1613-8insAC
NM_001270447.2:c.1748-9_1748-8insAC NP_001257376.1:n.1748-9_1748-8insAC
NM_001270448.2:c.1451-9_1451-8insAC NP_001257377.1:n.1451-9_1451-8insAC