Canonical Allele Identifier: CA397724955
Gene: ACADVL HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7127315A>T (hg19) chr17:g.7223996A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7223996A>T , CM000679.2:g.7223996A>T GRCh38
NC_000017.10:g.7127315A>T , CM000679.1:g.7127315A>T GRCh37
NC_000017.9:g.7068039A>T NCBI36
NG_007975.1:g.9163A>T
NG_008391.2:g.1055T>A
NG_033038.1:g.15549T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1361A>T MANE Select ENSP00000349297.5:p.Asp454Val
ENST00000322910.9:c.*1316A>T ENSP00000325395.5:n.*1316A>T
ENST00000350303.9:c.1295A>T ENSP00000344152.5:p.Asp432Val
ENST00000356839.9:c.1361A>T ENSP00000349297.5:p.Asp454Val
ENST00000542255.6:c.219A>T
ENST00000543245.6:c.1430A>T ENSP00000438689.2:p.Asp477Val
ENST00000578711.1:n.492A>T
ENST00000579425.5:n.477A>T
ENST00000579546.1:c.198A>T
ENST00000579894.5:n.72A>T
ENST00000583074.5:n.80A>T
ENST00000583850.5:n.136A>T
ENST00000583858.5:c.390A>T
ENST00000585203.6:n.552A>T
NM_000018.3:c.1361A>T NP_000009.1:p.Asp454Val
NM_001033859.2:c.1295A>T NP_001029031.1:p.Asp432Val
NM_001270447.1:c.1430A>T NP_001257376.1:p.Asp477Val
NM_001270448.1:c.1133A>T NP_001257377.1:p.Asp378Val
XM_006721516.2:c.1361A>T XP_006721579.2:p.Asp454Val
XM_011523829.1:c.1361A>T XP_011522131.1:p.Asp454Val
XM_011523830.1:c.1361A>T XP_011522132.1:p.Asp454Val
XR_934021.1:n.1468A>T
XR_934022.1:n.1468A>T
XR_934023.1:n.1468A>T
XM_006721516.3:c.1361A>T XP_006721579.2:p.Asp454Val
XM_011523829.2:c.1361A>T XP_011522131.1:p.Asp454Val
XM_011523830.2:c.1361A>T XP_011522132.1:p.Asp454Val
XM_024450741.1:c.1361A>T XP_024306509.1:p.Asp454Val
XR_934021.2:n.1420A>T
XR_934022.2:n.1420A>T
XR_934023.2:n.1420A>T
NM_000018.4:c.1361A>T MANE Select NP_000009.1:p.Asp454Val
NM_001033859.3:c.1295A>T NP_001029031.1:p.Asp432Val
NM_001270447.2:c.1430A>T NP_001257376.1:p.Asp477Val
NM_001270448.2:c.1133A>T NP_001257377.1:p.Asp378Val
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