Canonical Allele Identifier: CA497620020
Gene: ACADVL HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7125619C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222300C>A , CM000679.2:g.7222300C>A GRCh38
NC_000017.10:g.7125619C>A , CM000679.1:g.7125619C>A GRCh37
NC_000017.9:g.7066343C>A NCBI36
NG_007975.1:g.7467C>A
NG_008391.2:g.2751G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.876C>A MANE Select ENSP00000349297.5:p.Thr292=
ENST00000322910.9:c.*831C>A ENSP00000325395.5:n.*831C>A
ENST00000350303.9:c.810C>A ENSP00000344152.5:p.Thr270=
ENST00000356839.9:c.876C>A ENSP00000349297.5:p.Thr292=
ENST00000543245.6:c.945C>A ENSP00000438689.2:p.Thr315=
ENST00000577191.5:n.1048C>A
ENST00000581378.5:c.594C>A
ENST00000582379.1:n.260C>A
NM_000018.3:c.876C>A NP_000009.1:p.Thr292=
NM_001033859.2:c.810C>A NP_001029031.1:p.Thr270=
NM_001270447.1:c.945C>A NP_001257376.1:p.Thr315=
NM_001270448.1:c.648C>A NP_001257377.1:p.Thr216=
XM_006721516.2:c.876C>A XP_006721579.2:p.Thr292=
XM_011523829.1:c.876C>A XP_011522131.1:p.Thr292=
XM_011523830.1:c.876C>A XP_011522132.1:p.Thr292=
XR_934021.1:n.983C>A
XR_934022.1:n.983C>A
XR_934023.1:n.983C>A
XM_006721516.3:c.876C>A XP_006721579.2:p.Thr292=
XM_011523829.2:c.876C>A XP_011522131.1:p.Thr292=
XM_011523830.2:c.876C>A XP_011522132.1:p.Thr292=
XM_024450741.1:c.876C>A XP_024306509.1:p.Thr292=
XR_934021.2:n.935C>A
XR_934022.2:n.935C>A
XR_934023.2:n.935C>A
NM_000018.4:c.876C>A MANE Select NP_000009.1:p.Thr292=
NM_001033859.3:c.810C>A NP_001029031.1:p.Thr270=
NM_001270447.2:c.945C>A NP_001257376.1:p.Thr315=
NM_001270448.2:c.648C>A NP_001257377.1:p.Thr216=
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