Canonical Allele Identifier: CA497620158
Gene: ACADVL HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7125986T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222667T>C , CM000679.2:g.7222667T>C GRCh38
NC_000017.10:g.7125986T>C , CM000679.1:g.7125986T>C GRCh37
NC_000017.9:g.7066710T>C NCBI36
NG_007975.1:g.7834T>C
NG_008391.2:g.2384A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.879T>C MANE Select ENSP00000349297.5:p.His293=
ENST00000322910.9:c.*834T>C ENSP00000325395.5:n.*834T>C
ENST00000350303.9:c.813T>C ENSP00000344152.5:p.His271=
ENST00000356839.9:c.879T>C ENSP00000349297.5:p.His293=
ENST00000543245.6:c.948T>C ENSP00000438689.2:p.His316=
ENST00000578824.5:n.28T>C
ENST00000581378.5:c.597T>C
ENST00000582379.1:n.263T>C
NM_000018.3:c.879T>C NP_000009.1:p.His293=
NM_001033859.2:c.813T>C NP_001029031.1:p.His271=
NM_001270447.1:c.948T>C NP_001257376.1:p.His316=
NM_001270448.1:c.651T>C NP_001257377.1:p.His217=
XM_006721516.2:c.879T>C XP_006721579.2:p.His293=
XM_011523829.1:c.879T>C XP_011522131.1:p.His293=
XM_011523830.1:c.879T>C XP_011522132.1:p.His293=
XR_934021.1:n.986T>C
XR_934022.1:n.986T>C
XR_934023.1:n.986T>C
XM_006721516.3:c.879T>C XP_006721579.2:p.His293=
XM_011523829.2:c.879T>C XP_011522131.1:p.His293=
XM_011523830.2:c.879T>C XP_011522132.1:p.His293=
XM_024450741.1:c.879T>C XP_024306509.1:p.His293=
XR_934021.2:n.938T>C
XR_934022.2:n.938T>C
XR_934023.2:n.938T>C
NM_000018.4:c.879T>C MANE Select NP_000009.1:p.His293=
NM_001033859.3:c.813T>C NP_001029031.1:p.His271=
NM_001270447.2:c.948T>C NP_001257376.1:p.His316=
NM_001270448.2:c.651T>C NP_001257377.1:p.His217=
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