Canonical Allele Identifier: CA2808367426
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224267_7224268insCGTG , CM000679.2:g.7224267_7224268insCGTG GRCh38
NC_000017.10:g.7127586_7127587insCGTG , CM000679.1:g.7127586_7127587insCGTG GRCh37
NC_000017.9:g.7068310_7068311insCGTG NCBI36
NG_007975.1:g.9434_9435insCGTG
NG_008391.2:g.784_785insACGC
NG_033038.1:g.15278_15279insACGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1532+24_1532+25insCGTG MANE Select ENSP00000349297.5:n.1532+24_1532+25insCGTG
ENST00000322910.9:c.*1487+24_*1487+25insCGTG ENSP00000325395.5:n.*1487+24_*1487+25insCGTG
ENST00000350303.9:c.1466+24_1466+25insCGTG ENSP00000344152.5:n.1466+24_1466+25insCGTG
ENST00000356839.9:c.1532+24_1532+25insCGTG ENSP00000349297.5:n.1532+24_1532+25insCGTG
ENST00000542255.6:c.390+24_390+25insCGTG
ENST00000543245.6:c.1601+24_1601+25insCGTG ENSP00000438689.2:n.1601+24_1601+25insCGTG
ENST00000578319.5:n.27+24_27+25insCGTG
ENST00000578711.1:n.763_764insCGTG
ENST00000578809.5:n.51_52insCGTG
ENST00000579391.1:n.140+24_140+25insCGTG
ENST00000579425.5:n.648+24_648+25insCGTG
ENST00000579546.1:c.272-54_272-53insCGTG
ENST00000579894.5:n.319+24_319+25insCGTG
ENST00000583074.5:n.154-54_154-53insCGTG
ENST00000583850.5:n.307+24_307+25insCGTG
ENST00000583858.5:c.464-54_464-53insCGTG
ENST00000585203.6:n.723+24_723+25insCGTG
NM_000018.3:c.1532+24_1532+25insCGTG NP_000009.1:n.1532+24_1532+25insCGTG
NM_001033859.2:c.1466+24_1466+25insCGTG NP_001029031.1:n.1466+24_1466+25insCGTG
NM_001270447.1:c.1601+24_1601+25insCGTG NP_001257376.1:n.1601+24_1601+25insCGTG
NM_001270448.1:c.1304+24_1304+25insCGTG NP_001257377.1:n.1304+24_1304+25insCGTG
XM_006721516.2:c.1532+24_1532+25insCGTG XP_006721579.2:n.1532+24_1532+25insCGTG
XM_011523829.1:c.1435-54_1435-53insCGTG XP_011522131.1:n.1435-54_1435-53insCGTG
XM_011523830.1:c.1435-54_1435-53insCGTG XP_011522132.1:n.1435-54_1435-53insCGTG
XR_934021.1:n.1639+24_1639+25insCGTG
XR_934022.1:n.1542-54_1542-53insCGTG
XR_934023.1:n.1542-54_1542-53insCGTG
XM_006721516.3:c.1532+24_1532+25insCGTG XP_006721579.2:n.1532+24_1532+25insCGTG
XM_011523829.2:c.1435-54_1435-53insCGTG XP_011522131.1:n.1435-54_1435-53insCGTG
XM_011523830.2:c.1435-54_1435-53insCGTG XP_011522132.1:n.1435-54_1435-53insCGTG
XM_024450741.1:c.1435-54_1435-53insCGTG XP_024306509.1:n.1435-54_1435-53insCGTG
XR_934021.2:n.1591+24_1591+25insCGTG
XR_934022.2:n.1494-54_1494-53insCGTG
XR_934023.2:n.1494-54_1494-53insCGTG
NM_000018.4:c.1532+24_1532+25insCGTG MANE Select NP_000009.1:n.1532+24_1532+25insCGTG
NM_001033859.3:c.1466+24_1466+25insCGTG NP_001029031.1:n.1466+24_1466+25insCGTG
NM_001270447.2:c.1601+24_1601+25insCGTG NP_001257376.1:n.1601+24_1601+25insCGTG
NM_001270448.2:c.1304+24_1304+25insCGTG NP_001257377.1:n.1304+24_1304+25insCGTG