Canonical Allele Identifier: CA397724186
Gene: ACADVL HGNC NCBI

Linked Data

ClinVar Variation Id: 592247
ClinVar RCV Id: RCV000727590 RCV001200831 RCV003489845
dbSNP Id: rs1356652354
gnomAD v3: 17-7222812-T-C
gnomAD v4: 17-7222812-T-C
MyVariant Identifiers: chr17:g.7126131T>C (hg19) chr17:g.7222812T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222812T>C , CM000679.2:g.7222812T>C GRCh38
NC_000017.10:g.7126131T>C , CM000679.1:g.7126131T>C GRCh37
NC_000017.9:g.7066855T>C NCBI36
NG_007975.1:g.7979T>C
NG_008391.2:g.2239A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1024T>C MANE Select ENSP00000349297.5:p.Phe342Leu
ENST00000322910.9:c.*979T>C ENSP00000325395.5:n.*979T>C
ENST00000350303.9:c.958T>C ENSP00000344152.5:p.Phe320Leu
ENST00000356839.9:c.1024T>C ENSP00000349297.5:p.Phe342Leu
ENST00000543245.6:c.1093T>C ENSP00000438689.2:p.Phe365Leu
ENST00000578824.5:n.173T>C
ENST00000581378.5:c.742T>C
ENST00000582379.1:n.408T>C
ENST00000583858.5:c.53T>C
NM_000018.3:c.1024T>C NP_000009.1:p.Phe342Leu
NM_001033859.2:c.958T>C NP_001029031.1:p.Phe320Leu
NM_001270447.1:c.1093T>C NP_001257376.1:p.Phe365Leu
NM_001270448.1:c.796T>C NP_001257377.1:p.Phe266Leu
XM_006721516.2:c.1024T>C XP_006721579.2:p.Phe342Leu
XM_011523829.1:c.1024T>C XP_011522131.1:p.Phe342Leu
XM_011523830.1:c.1024T>C XP_011522132.1:p.Phe342Leu
XR_934021.1:n.1131T>C
XR_934022.1:n.1131T>C
XR_934023.1:n.1131T>C
XM_006721516.3:c.1024T>C XP_006721579.2:p.Phe342Leu
XM_011523829.2:c.1024T>C XP_011522131.1:p.Phe342Leu
XM_011523830.2:c.1024T>C XP_011522132.1:p.Phe342Leu
XM_024450741.1:c.1024T>C XP_024306509.1:p.Phe342Leu
XR_934021.2:n.1083T>C
XR_934022.2:n.1083T>C
XR_934023.2:n.1083T>C
NM_000018.4:c.1024T>C MANE Select NP_000009.1:p.Phe342Leu
NM_001033859.3:c.958T>C NP_001029031.1:p.Phe320Leu
NM_001270447.2:c.1093T>C NP_001257376.1:p.Phe365Leu
NM_001270448.2:c.796T>C NP_001257377.1:p.Phe266Leu
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