Canonical Allele Identifier: CA2580094847
Gene: ACADVL HGNC NCBI

Linked Data

ClinVar Variation Id: 2104994
ClinVar RCV Id: RCV003041830

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224526_7224527dup , CM000679.2:g.7224526_7224527dup GRCh38
NC_000017.10:g.7127845_7127846dup , CM000679.1:g.7127845_7127846dup GRCh37
NC_000017.9:g.7068569_7068570dup NCBI36
NG_007975.1:g.9693_9694dup
NG_008391.2:g.524_525dup
NG_033038.1:g.15018_15019dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1652_1653dup MANE Select ENSP00000349297.5:p.Ile552Ter
ENST00000322910.9:c.*1607_*1608dup ENSP00000325395.5:n.*1607_*1608dup
ENST00000350303.9:c.1586_1587dup ENSP00000344152.5:p.Ile530Ter
ENST00000356839.9:c.1652_1653dup ENSP00000349297.5:p.Ile552Ter
ENST00000542255.6:c.510_511dup
ENST00000543245.6:c.1721_1722dup ENSP00000438689.2:p.Ile575Ter
ENST00000578319.5:n.233_234dup
ENST00000578711.1:n.1022_1023dup
ENST00000578809.5:n.224_225dup
ENST00000579391.1:n.256_257dup
ENST00000579425.5:n.768_769dup
ENST00000579546.1:c.387_388dup
ENST00000582450.1:n.160_161dup
ENST00000583074.5:n.273_274dup
ENST00000583848.5:c.38_39dup ENSP00000466487.1:p.Ile14Ter
ENST00000583850.5:n.423_424dup
ENST00000583858.5:c.583_584dup
ENST00000585203.6:n.843_844dup
NM_000018.3:c.1652_1653dup NP_000009.1:p.Ile552Ter
NM_001033859.2:c.1586_1587dup NP_001029031.1:p.Ile530Ter
NM_001270447.1:c.1721_1722dup NP_001257376.1:p.Ile575Ter
NM_001270448.1:c.1424_1425dup NP_001257377.1:p.Ile476Ter
XM_006721516.2:c.1652_1653dup XP_006721579.2:p.Ile552Ter
XM_011523829.1:c.1550_1551dup XP_011522131.1:p.Ile518Ter
XM_011523830.1:c.1550_1551dup XP_011522132.1:p.Ile518Ter
XR_934021.1:n.1755_1756dup
XR_934022.1:n.1661_1662dup
XR_934023.1:n.1661_1662dup
XM_006721516.3:c.1652_1653dup XP_006721579.2:p.Ile552Ter
XM_011523829.2:c.1550_1551dup XP_011522131.1:p.Ile518Ter
XM_011523830.2:c.1550_1551dup XP_011522132.1:p.Ile518Ter
XM_024450741.1:c.1640_1641dup XP_024306509.1:p.Ile548Ter
XR_934021.2:n.1707_1708dup
XR_934022.2:n.1613_1614dup
XR_934023.2:n.1613_1614dup
NM_000018.4:c.1652_1653dup MANE Select NP_000009.1:p.Ile552Ter
NM_001033859.3:c.1586_1587dup NP_001029031.1:p.Ile530Ter
NM_001270447.2:c.1721_1722dup NP_001257376.1:p.Ile575Ter
NM_001270448.2:c.1424_1425dup NP_001257377.1:p.Ile476Ter