Canonical Allele Identifier: CA2245714655
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224556_7224557delinsAG , CM000679.2:g.7224556_7224557delinsAG GRCh38
NC_000017.10:g.7127875_7127876delinsAG , CM000679.1:g.7127875_7127876delinsAG GRCh37
NC_000017.9:g.7068599_7068600delinsAG NCBI36
NG_007975.1:g.9723_9724delinsAG
NG_008391.2:g.494_495delinsCT
NG_033038.1:g.14988_14989delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1678+4_1678+5delinsAG MANE Select ENSP00000349297.5:n.1678+4_1678+5delinsAG
ENST00000322910.9:c.*1633+4_*1633+5delinsAG ENSP00000325395.5:n.*1633+4_*1633+5delinsAG
ENST00000350303.9:c.1612+4_1612+5delinsAG ENSP00000344152.5:n.1612+4_1612+5delinsAG
ENST00000356839.9:c.1678+4_1678+5delinsAG ENSP00000349297.5:n.1678+4_1678+5delinsAG
ENST00000542255.6:c.536+4_536+5delinsAG
ENST00000543245.6:c.1747+4_1747+5delinsAG ENSP00000438689.2:n.1747+4_1747+5delinsAG
ENST00000578319.5:n.259+4_259+5delinsAG
ENST00000578711.1:n.1052_1053delinsAG
ENST00000578809.5:n.250+4_250+5delinsAG
ENST00000579391.1:n.286_287delinsAG
ENST00000579425.5:n.794+4_794+5delinsAG
ENST00000579546.1:c.413+4_413+5delinsAG
ENST00000582450.1:n.190_191delinsAG
ENST00000583074.5:n.299+4_299+5delinsAG
ENST00000583848.5:c.64+4_64+5delinsAG ENSP00000466487.1:n.64+4_64+5delinsAG
ENST00000583850.5:n.449+4_449+5delinsAG
ENST00000583858.5:c.609+4_609+5delinsAG
ENST00000585203.6:n.869+4_869+5delinsAG
NM_000018.3:c.1678+4_1678+5delinsAG NP_000009.1:n.1678+4_1678+5delinsAG
NM_001033859.2:c.1612+4_1612+5delinsAG NP_001029031.1:n.1612+4_1612+5delinsAG
NM_001270447.1:c.1747+4_1747+5delinsAG NP_001257376.1:n.1747+4_1747+5delinsAG
NM_001270448.1:c.1450+4_1450+5delinsAG NP_001257377.1:n.1450+4_1450+5delinsAG
XM_006721516.2:c.1678+4_1678+5delinsAG XP_006721579.2:n.1678+4_1678+5delinsAG
XM_011523829.1:c.1576+4_1576+5delinsAG XP_011522131.1:n.1576+4_1576+5delinsAG
XM_011523830.1:c.1576+4_1576+5delinsAG XP_011522132.1:n.1576+4_1576+5delinsAG
XR_934021.1:n.1781+4_1781+5delinsAG
XR_934022.1:n.1687+4_1687+5delinsAG
XR_934023.1:n.1687+4_1687+5delinsAG
XM_006721516.3:c.1678+4_1678+5delinsAG XP_006721579.2:n.1678+4_1678+5delinsAG
XM_011523829.2:c.1576+4_1576+5delinsAG XP_011522131.1:n.1576+4_1576+5delinsAG
XM_011523830.2:c.1576+4_1576+5delinsAG XP_011522132.1:n.1576+4_1576+5delinsAG
XM_024450741.1:c.1666+4_1666+5delinsAG XP_024306509.1:n.1666+4_1666+5delinsAG
XR_934021.2:n.1733+4_1733+5delinsAG
XR_934022.2:n.1639+4_1639+5delinsAG
XR_934023.2:n.1639+4_1639+5delinsAG
NM_000018.4:c.1678+4_1678+5delinsAG MANE Select NP_000009.1:n.1678+4_1678+5delinsAG
NM_001033859.3:c.1612+4_1612+5delinsAG NP_001029031.1:n.1612+4_1612+5delinsAG
NM_001270447.2:c.1747+4_1747+5delinsAG NP_001257376.1:n.1747+4_1747+5delinsAG
NM_001270448.2:c.1450+4_1450+5delinsAG NP_001257377.1:n.1450+4_1450+5delinsAG