Canonical Allele Identifier: CA497694178
Gene: ACADVL HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7127158A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7223839A>G , CM000679.2:g.7223839A>G GRCh38
NC_000017.10:g.7127158A>G , CM000679.1:g.7127158A>G GRCh37
NC_000017.9:g.7067882A>G NCBI36
NG_007975.1:g.9006A>G
NG_008391.2:g.1212T>C
NG_033038.1:g.15706T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000356839.10:c.1296A>G MANE Select ENSP00000349297.5:p.Glu432=
ENST00000322910.9:c.*1251A>G ENSP00000325395.5:n.*1251A>G
ENST00000350303.9:c.1230A>G ENSP00000344152.5:p.Glu410=
ENST00000356839.9:c.1296A>G ENSP00000349297.5:p.Glu432=
ENST00000542255.6:c.154A>G
ENST00000543245.6:c.1365A>G ENSP00000438689.2:p.Glu455=
ENST00000578711.1:n.335A>G
ENST00000578824.5:n.712A>G
ENST00000579425.5:n.320A>G
ENST00000579546.1:c.133A>G
ENST00000583074.5:n.15A>G
ENST00000583850.5:n.71A>G
ENST00000583858.5:c.325A>G
ENST00000585203.6:n.504A>G
NM_000018.3:c.1296A>G NP_000009.1:p.Glu432=
NM_001033859.2:c.1230A>G NP_001029031.1:p.Glu410=
NM_001270447.1:c.1365A>G NP_001257376.1:p.Glu455=
NM_001270448.1:c.1068A>G NP_001257377.1:p.Glu356=
XM_006721516.2:c.1296A>G XP_006721579.2:p.Glu432=
XM_011523829.1:c.1296A>G XP_011522131.1:p.Glu432=
XM_011523830.1:c.1296A>G XP_011522132.1:p.Glu432=
XR_934021.1:n.1403A>G
XR_934022.1:n.1403A>G
XR_934023.1:n.1403A>G
XM_006721516.3:c.1296A>G XP_006721579.2:p.Glu432=
XM_011523829.2:c.1296A>G XP_011522131.1:p.Glu432=
XM_011523830.2:c.1296A>G XP_011522132.1:p.Glu432=
XM_024450741.1:c.1296A>G XP_024306509.1:p.Glu432=
XR_934021.2:n.1355A>G
XR_934022.2:n.1355A>G
XR_934023.2:n.1355A>G
NM_000018.4:c.1296A>G MANE Select NP_000009.1:p.Glu432=
NM_001033859.3:c.1230A>G NP_001029031.1:p.Glu410=
NM_001270447.2:c.1365A>G NP_001257376.1:p.Glu455=
NM_001270448.2:c.1068A>G NP_001257377.1:p.Glu356=