Canonical Allele Identifier: CA8337899
Gene: ACADVL HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 371464
ClinVar RCV Id: RCV000409715

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222669_7222672dup , CM000679.2:g.7222669_7222672dup GRCh38
NC_000017.10:g.7125988_7125991dup , CM000679.1:g.7125988_7125991dup GRCh37
NC_000017.9:g.7066712_7066715dup NCBI36
NG_007975.1:g.7836_7839dup
NG_008391.2:g.2379_2382dup

Transcript Alleles

HGVS Amino-acid change
NM_000018.3:c.881_884dup VV
NM_001033859.2:c.815_818dup VV
NM_001270447.1:c.950_953dup VV
NM_001270448.1:c.653_656dup VV
XM_006721516.2:c.881_884dup
XM_011523829.1:c.881_884dup
XM_011523830.1:c.881_884dup
XR_934021.1:n.988_991dup
XR_934022.1:n.988_991dup
XR_934023.1:n.988_991dup
XM_006721516.3:c.881_884dup
XM_011523829.2:c.881_884dup
XM_011523830.2:c.881_884dup
XM_024450741.1:c.881_884dup
XR_934021.2:n.940_943dup
XR_934022.2:n.940_943dup
XR_934023.2:n.940_943dup
NM_000018.4:c.881_884dup VV MANE Preferred
ENST00000322910.9:c.*836_*839dup ENSP00000325395.5:p.=
ENST00000350303.9:c.815_818dup
ENST00000356839.9:c.881_884dup
ENST00000543245.6:c.950_953dup
ENST00000578824.5:n.30_33dup
ENST00000581378.5:n.599_602dup
ENST00000582379.1:n.265_268dup