Canonical Allele Identifier: CA497694011
Gene: ACADVL HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7125320T>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222001T>C , CM000679.2:g.7222001T>C GRCh38
NC_000017.10:g.7125320T>C , CM000679.1:g.7125320T>C GRCh37
NC_000017.9:g.7066044T>C NCBI36
NG_007975.1:g.7168T>C
NG_008391.2:g.3050A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.672T>C MANE Select ENSP00000349297.5:p.Asp224=
ENST00000322910.9:c.*627T>C ENSP00000325395.5:n.*627T>C
ENST00000350303.9:c.606T>C ENSP00000344152.5:p.Asp202=
ENST00000356839.9:c.672T>C ENSP00000349297.5:p.Asp224=
ENST00000543245.6:c.741T>C ENSP00000438689.2:p.Asp247=
ENST00000577191.5:n.749T>C
ENST00000577857.5:n.488T>C
ENST00000579286.5:n.853T>C
ENST00000580365.1:n.403T>C
ENST00000581378.5:c.390T>C
ENST00000582379.1:n.56T>C
ENST00000583760.1:n.454T>C
NM_000018.3:c.672T>C NP_000009.1:p.Asp224=
NM_001033859.2:c.606T>C NP_001029031.1:p.Asp202=
NM_001270447.1:c.741T>C NP_001257376.1:p.Asp247=
NM_001270448.1:c.444T>C NP_001257377.1:p.Asp148=
XM_006721516.2:c.672T>C XP_006721579.2:p.Asp224=
XM_011523829.1:c.672T>C XP_011522131.1:p.Asp224=
XM_011523830.1:c.672T>C XP_011522132.1:p.Asp224=
XR_934021.1:n.779T>C
XR_934022.1:n.779T>C
XR_934023.1:n.779T>C
XM_006721516.3:c.672T>C XP_006721579.2:p.Asp224=
XM_011523829.2:c.672T>C XP_011522131.1:p.Asp224=
XM_011523830.2:c.672T>C XP_011522132.1:p.Asp224=
XM_024450741.1:c.672T>C XP_024306509.1:p.Asp224=
XR_934021.2:n.731T>C
XR_934022.2:n.731T>C
XR_934023.2:n.731T>C
NM_000018.4:c.672T>C MANE Select NP_000009.1:p.Asp224=
NM_001033859.3:c.606T>C NP_001029031.1:p.Asp202=
NM_001270447.2:c.741T>C NP_001257376.1:p.Asp247=
NM_001270448.2:c.444T>C NP_001257377.1:p.Asp148=
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