Canonical Allele Identifier: CA497694278
Gene: ACADVL HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7127524T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224205T>C , CM000679.2:g.7224205T>C GRCh38
NC_000017.10:g.7127524T>C , CM000679.1:g.7127524T>C GRCh37
NC_000017.9:g.7068248T>C NCBI36
NG_007975.1:g.9372T>C
NG_008391.2:g.846A>G
NG_033038.1:g.15340A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1494T>C MANE Select ENSP00000349297.5:p.Ala498=
ENST00000322910.9:c.*1449T>C ENSP00000325395.5:n.*1449T>C
ENST00000350303.9:c.1428T>C ENSP00000344152.5:p.Ala476=
ENST00000356839.9:c.1494T>C ENSP00000349297.5:p.Ala498=
ENST00000542255.6:c.352T>C
ENST00000543245.6:c.1563T>C ENSP00000438689.2:p.Ala521=
ENST00000578711.1:n.701T>C
ENST00000579391.1:n.102T>C
ENST00000579425.5:n.610T>C
ENST00000579546.1:c.272-116T>C
ENST00000579894.5:n.281T>C
ENST00000583074.5:n.154-116T>C
ENST00000583850.5:n.269T>C
ENST00000583858.5:c.464-116T>C
ENST00000585203.6:n.685T>C
NM_000018.3:c.1494T>C NP_000009.1:p.Ala498=
NM_001033859.2:c.1428T>C NP_001029031.1:p.Ala476=
NM_001270447.1:c.1563T>C NP_001257376.1:p.Ala521=
NM_001270448.1:c.1266T>C NP_001257377.1:p.Ala422=
XM_006721516.2:c.1494T>C XP_006721579.2:p.Ala498=
XM_011523829.1:c.1435-116T>C XP_011522131.1:n.1435-116T>C
XM_011523830.1:c.1435-116T>C XP_011522132.1:n.1435-116T>C
XR_934021.1:n.1601T>C
XR_934022.1:n.1542-116T>C
XR_934023.1:n.1542-116T>C
XM_006721516.3:c.1494T>C XP_006721579.2:p.Ala498=
XM_011523829.2:c.1435-116T>C XP_011522131.1:n.1435-116T>C
XM_011523830.2:c.1435-116T>C XP_011522132.1:n.1435-116T>C
XM_024450741.1:c.1435-116T>C XP_024306509.1:n.1435-116T>C
XR_934021.2:n.1553T>C
XR_934022.2:n.1494-116T>C
XR_934023.2:n.1494-116T>C
NM_000018.4:c.1494T>C MANE Select NP_000009.1:p.Ala498=
NM_001033859.3:c.1428T>C NP_001029031.1:p.Ala476=
NM_001270447.2:c.1563T>C NP_001257376.1:p.Ala521=
NM_001270448.2:c.1266T>C NP_001257377.1:p.Ala422=
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