Canonical Allele Identifier: CA397723920
Gene: ACADVL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222683A>C , CM000679.2:g.7222683A>C GRCh38
NC_000017.10:g.7126002A>C , CM000679.1:g.7126002A>C GRCh37
NC_000017.9:g.7066726A>C NCBI36
NG_007975.1:g.7850A>C
NG_008391.2:g.2368T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.895A>C MANE Select ENSP00000349297.5:p.Lys299Gln
ENST00000322910.9:c.*850A>C ENSP00000325395.5:n.*850A>C
ENST00000350303.9:c.829A>C ENSP00000344152.5:p.Lys277Gln
ENST00000356839.9:c.895A>C ENSP00000349297.5:p.Lys299Gln
ENST00000543245.6:c.964A>C ENSP00000438689.2:p.Lys322Gln
ENST00000578824.5:n.44A>C
ENST00000581378.5:c.613A>C
ENST00000582379.1:n.279A>C
NM_000018.3:c.895A>C NP_000009.1:p.Lys299Gln
NM_001033859.2:c.829A>C NP_001029031.1:p.Lys277Gln
NM_001270447.1:c.964A>C NP_001257376.1:p.Lys322Gln
NM_001270448.1:c.667A>C NP_001257377.1:p.Lys223Gln
XM_006721516.2:c.895A>C XP_006721579.2:p.Lys299Gln
XM_011523829.1:c.895A>C XP_011522131.1:p.Lys299Gln
XM_011523830.1:c.895A>C XP_011522132.1:p.Lys299Gln
XR_934021.1:n.1002A>C
XR_934022.1:n.1002A>C
XR_934023.1:n.1002A>C
XM_006721516.3:c.895A>C XP_006721579.2:p.Lys299Gln
XM_011523829.2:c.895A>C XP_011522131.1:p.Lys299Gln
XM_011523830.2:c.895A>C XP_011522132.1:p.Lys299Gln
XM_024450741.1:c.895A>C XP_024306509.1:p.Lys299Gln
XR_934021.2:n.954A>C
XR_934022.2:n.954A>C
XR_934023.2:n.954A>C
NM_000018.4:c.895A>C MANE Select NP_000009.1:p.Lys299Gln
NM_001033859.3:c.829A>C NP_001029031.1:p.Lys277Gln
NM_001270447.2:c.964A>C NP_001257376.1:p.Lys322Gln
NM_001270448.2:c.667A>C NP_001257377.1:p.Lys223Gln