Canonical Allele Identifier: CA397723368
Gene: ACADVL HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7125288T>C (hg19) chr17:g.7221969T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221969T>C , CM000679.2:g.7221969T>C GRCh38
NC_000017.10:g.7125288T>C , CM000679.1:g.7125288T>C GRCh37
NC_000017.9:g.7066012T>C NCBI36
NG_007975.1:g.7136T>C
NG_008391.2:g.3082A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.640T>C MANE Select ENSP00000349297.5:p.Phe214Leu
ENST00000322910.9:c.*595T>C ENSP00000325395.5:n.*595T>C
ENST00000350303.9:c.574T>C ENSP00000344152.5:p.Phe192Leu
ENST00000356839.9:c.640T>C ENSP00000349297.5:p.Phe214Leu
ENST00000543245.6:c.709T>C ENSP00000438689.2:p.Phe237Leu
ENST00000577191.5:n.717T>C
ENST00000577857.5:n.456T>C
ENST00000579286.5:n.821T>C
ENST00000580365.1:n.371T>C
ENST00000581378.5:c.358T>C
ENST00000581562.5:n.542T>C
ENST00000582379.1:n.24T>C
ENST00000583312.5:c.655T>C ENSP00000467920.1:p.Phe219Leu
ENST00000583760.1:n.422T>C
NM_000018.3:c.640T>C NP_000009.1:p.Phe214Leu
NM_001033859.2:c.574T>C NP_001029031.1:p.Phe192Leu
NM_001270447.1:c.709T>C NP_001257376.1:p.Phe237Leu
NM_001270448.1:c.412T>C NP_001257377.1:p.Phe138Leu
XM_006721516.2:c.640T>C XP_006721579.2:p.Phe214Leu
XM_011523829.1:c.640T>C XP_011522131.1:p.Phe214Leu
XM_011523830.1:c.640T>C XP_011522132.1:p.Phe214Leu
XR_934021.1:n.747T>C
XR_934022.1:n.747T>C
XR_934023.1:n.747T>C
XM_006721516.3:c.640T>C XP_006721579.2:p.Phe214Leu
XM_011523829.2:c.640T>C XP_011522131.1:p.Phe214Leu
XM_011523830.2:c.640T>C XP_011522132.1:p.Phe214Leu
XM_024450741.1:c.640T>C XP_024306509.1:p.Phe214Leu
XR_934021.2:n.699T>C
XR_934022.2:n.699T>C
XR_934023.2:n.699T>C
NM_000018.4:c.640T>C MANE Select NP_000009.1:p.Phe214Leu
NM_001033859.3:c.574T>C NP_001029031.1:p.Phe192Leu
NM_001270447.2:c.709T>C NP_001257376.1:p.Phe237Leu
NM_001270448.2:c.412T>C NP_001257377.1:p.Phe138Leu
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