Canonical Allele Identifier: CA497619969
Gene: ACADVL HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7125580C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222261C>T , CM000679.2:g.7222261C>T GRCh38
NC_000017.10:g.7125580C>T , CM000679.1:g.7125580C>T GRCh37
NC_000017.9:g.7066304C>T NCBI36
NG_007975.1:g.7428C>T
NG_008391.2:g.2790G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.837C>T MANE Select ENSP00000349297.5:p.Ile279=
ENST00000322910.9:c.*792C>T ENSP00000325395.5:n.*792C>T
ENST00000350303.9:c.771C>T ENSP00000344152.5:p.Ile257=
ENST00000356839.9:c.837C>T ENSP00000349297.5:p.Ile279=
ENST00000543245.6:c.906C>T ENSP00000438689.2:p.Ile302=
ENST00000577191.5:n.1009C>T
ENST00000581378.5:c.555C>T
ENST00000582379.1:n.221C>T
NM_000018.3:c.837C>T NP_000009.1:p.Ile279=
NM_001033859.2:c.771C>T NP_001029031.1:p.Ile257=
NM_001270447.1:c.906C>T NP_001257376.1:p.Ile302=
NM_001270448.1:c.609C>T NP_001257377.1:p.Ile203=
XM_006721516.2:c.837C>T XP_006721579.2:p.Ile279=
XM_011523829.1:c.837C>T XP_011522131.1:p.Ile279=
XM_011523830.1:c.837C>T XP_011522132.1:p.Ile279=
XR_934021.1:n.944C>T
XR_934022.1:n.944C>T
XR_934023.1:n.944C>T
XM_006721516.3:c.837C>T XP_006721579.2:p.Ile279=
XM_011523829.2:c.837C>T XP_011522131.1:p.Ile279=
XM_011523830.2:c.837C>T XP_011522132.1:p.Ile279=
XM_024450741.1:c.837C>T XP_024306509.1:p.Ile279=
XR_934021.2:n.896C>T
XR_934022.2:n.896C>T
XR_934023.2:n.896C>T
NM_000018.4:c.837C>T MANE Select NP_000009.1:p.Ile279=
NM_001033859.3:c.771C>T NP_001029031.1:p.Ile257=
NM_001270447.2:c.906C>T NP_001257376.1:p.Ile302=
NM_001270448.2:c.609C>T NP_001257377.1:p.Ile203=
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