Canonical Allele Identifier: CA2245711869
Gene: ACADVL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7223783A= , CM000679.2:g.7223783A= GRCh38
NC_000017.10:g.7127102A= , CM000679.1:g.7127102A= GRCh37
NC_000017.9:g.7067826A= NCBI36
NG_007975.1:g.8950A=
NG_008391.2:g.1268T=
NG_033038.1:g.15762T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1270-30A= MANE Select ENSP00000349297.5:n.1270-30A=
ENST00000322910.9:c.*1225-30A= ENSP00000325395.5:n.*1225-30A=
ENST00000350303.9:c.1204-30A= ENSP00000344152.5:n.1204-30A=
ENST00000356839.9:c.1270-30A= ENSP00000349297.5:n.1270-30A=
ENST00000542255.6:c.128-30A=
ENST00000543245.6:c.1339-30A= ENSP00000438689.2:n.1339-30A=
ENST00000578579.2:n.441-30A=
ENST00000578711.1:n.279A=
ENST00000578824.5:n.686-30A=
ENST00000579425.5:n.294-30A=
ENST00000579546.1:c.107-30A=
ENST00000583850.5:n.45-30A=
ENST00000583858.5:c.299-30A=
ENST00000585203.6:n.478-30A=
NM_000018.3:c.1270-30A= NP_000009.1:n.1270-30A=
NM_001033859.2:c.1204-30A= NP_001029031.1:n.1204-30A=
NM_001270447.1:c.1339-30A= NP_001257376.1:n.1339-30A=
NM_001270448.1:c.1042-30A= NP_001257377.1:n.1042-30A=
XM_006721516.2:c.1270-30A= XP_006721579.2:n.1270-30A=
XM_011523829.1:c.1270-30A= XP_011522131.1:n.1270-30A=
XM_011523830.1:c.1270-30A= XP_011522132.1:n.1270-30A=
XR_934021.1:n.1377-30A=
XR_934022.1:n.1377-30A=
XR_934023.1:n.1377-30A=
XM_006721516.3:c.1270-30A= XP_006721579.2:n.1270-30A=
XM_011523829.2:c.1270-30A= XP_011522131.1:n.1270-30A=
XM_011523830.2:c.1270-30A= XP_011522132.1:n.1270-30A=
XM_024450741.1:c.1270-30A= XP_024306509.1:n.1270-30A=
XR_934021.2:n.1329-30A=
XR_934022.2:n.1329-30A=
XR_934023.2:n.1329-30A=
NM_000018.4:c.1270-30A= MANE Select NP_000009.1:n.1270-30A=
NM_001033859.3:c.1204-30A= NP_001029031.1:n.1204-30A=
NM_001270447.2:c.1339-30A= NP_001257376.1:n.1339-30A=
NM_001270448.2:c.1042-30A= NP_001257377.1:n.1042-30A=
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