Canonical Allele Identifier: CA497619870
Gene: ACADVL HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7125538A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222219A>C , CM000679.2:g.7222219A>C GRCh38
NC_000017.10:g.7125538A>C , CM000679.1:g.7125538A>C GRCh37
NC_000017.9:g.7066262A>C NCBI36
NG_007975.1:g.7386A>C
NG_008391.2:g.2832T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.795A>C MANE Select ENSP00000349297.5:p.Thr265=
ENST00000322910.9:c.*750A>C ENSP00000325395.5:n.*750A>C
ENST00000350303.9:c.729A>C ENSP00000344152.5:p.Thr243=
ENST00000356839.9:c.795A>C ENSP00000349297.5:p.Thr265=
ENST00000543245.6:c.864A>C ENSP00000438689.2:p.Thr288=
ENST00000577191.5:n.967A>C
ENST00000581378.5:c.513A>C
ENST00000582379.1:n.179A>C
NM_000018.3:c.795A>C NP_000009.1:p.Thr265=
NM_001033859.2:c.729A>C NP_001029031.1:p.Thr243=
NM_001270447.1:c.864A>C NP_001257376.1:p.Thr288=
NM_001270448.1:c.567A>C NP_001257377.1:p.Thr189=
XM_006721516.2:c.795A>C XP_006721579.2:p.Thr265=
XM_011523829.1:c.795A>C XP_011522131.1:p.Thr265=
XM_011523830.1:c.795A>C XP_011522132.1:p.Thr265=
XR_934021.1:n.902A>C
XR_934022.1:n.902A>C
XR_934023.1:n.902A>C
XM_006721516.3:c.795A>C XP_006721579.2:p.Thr265=
XM_011523829.2:c.795A>C XP_011522131.1:p.Thr265=
XM_011523830.2:c.795A>C XP_011522132.1:p.Thr265=
XM_024450741.1:c.795A>C XP_024306509.1:p.Thr265=
XR_934021.2:n.854A>C
XR_934022.2:n.854A>C
XR_934023.2:n.854A>C
NM_000018.4:c.795A>C MANE Select NP_000009.1:p.Thr265=
NM_001033859.3:c.729A>C NP_001029031.1:p.Thr243=
NM_001270447.2:c.864A>C NP_001257376.1:p.Thr288=
NM_001270448.2:c.567A>C NP_001257377.1:p.Thr189=