Canonical Allele Identifier: CA2245714855
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224608C= , CM000679.2:g.7224608C= GRCh38
NC_000017.10:g.7127927C= , CM000679.1:g.7127927C= GRCh37
NC_000017.9:g.7068651C= NCBI36
NG_007975.1:g.9775C=
NG_008391.2:g.443G=
NG_033038.1:g.14937G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1679-34C= MANE Select ENSP00000349297.5:n.1679-34C=
ENST00000322910.9:c.*1634-34C= ENSP00000325395.5:n.*1634-34C=
ENST00000350303.9:c.1613-34C= ENSP00000344152.5:n.1613-34C=
ENST00000356839.9:c.1679-34C= ENSP00000349297.5:n.1679-34C=
ENST00000542255.6:c.536+56C=
ENST00000543245.6:c.1748-34C= ENSP00000438689.2:n.1748-34C=
ENST00000578319.5:n.260-34C=
ENST00000578711.1:n.1104C=
ENST00000578809.5:n.251-34C=
ENST00000579391.1:n.338C=
ENST00000579425.5:n.795-34C=
ENST00000579546.1:c.414-34C=
ENST00000582450.1:n.242C=
ENST00000583074.5:n.299+56C=
ENST00000583848.5:c.65-54C= ENSP00000466487.1:n.65-54C=
ENST00000583850.5:n.450-34C=
ENST00000583858.5:c.610-34C=
ENST00000585203.6:n.870-34C=
NM_000018.3:c.1679-34C= NP_000009.1:n.1679-34C=
NM_001033859.2:c.1613-34C= NP_001029031.1:n.1613-34C=
NM_001270447.1:c.1748-34C= NP_001257376.1:n.1748-34C=
NM_001270448.1:c.1451-34C= NP_001257377.1:n.1451-34C=
XM_006721516.2:c.1678+56C= XP_006721579.2:n.1678+56C=
XM_011523829.1:c.1576+56C= XP_011522131.1:n.1576+56C=
XM_011523830.1:c.1577-34C= XP_011522132.1:n.1577-34C=
XR_934021.1:n.1782-34C=
XR_934022.1:n.1688-34C=
XR_934023.1:n.1687+56C=
XM_006721516.3:c.1678+56C= XP_006721579.2:n.1678+56C=
XM_011523829.2:c.1576+56C= XP_011522131.1:n.1576+56C=
XM_011523830.2:c.1577-34C= XP_011522132.1:n.1577-34C=
XM_024450741.1:c.1667-34C= XP_024306509.1:n.1667-34C=
XR_934021.2:n.1734-34C=
XR_934022.2:n.1640-34C=
XR_934023.2:n.1639+56C=
NM_000018.4:c.1679-34C= MANE Select NP_000009.1:n.1679-34C=
NM_001033859.3:c.1613-34C= NP_001029031.1:n.1613-34C=
NM_001270447.2:c.1748-34C= NP_001257376.1:n.1748-34C=
NM_001270448.2:c.1451-34C= NP_001257377.1:n.1451-34C=