Canonical Allele Identifier: CA397723165
Gene: ACADVL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221620A>C , CM000679.2:g.7221620A>C GRCh38
NC_000017.10:g.7124939A>C , CM000679.1:g.7124939A>C GRCh37
NC_000017.9:g.7065663A>C NCBI36
NG_007975.1:g.6787A>C
NG_008391.2:g.3431T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000356839.10:c.560A>C MANE Select ENSP00000349297.5:p.Lys187Thr
ENST00000322910.9:c.*515A>C ENSP00000325395.5:p.=
ENST00000350303.9:c.494A>C ENSP00000344152.5:p.Lys165Thr
ENST00000356839.9:c.560A>C ENSP00000349297.5:p.Lys187Thr
ENST00000543245.6:c.629A>C ENSP00000438689.2:p.Lys210Thr
ENST00000577191.5:n.637A>C
ENST00000577433.5:n.768A>C
ENST00000577857.5:n.376A>C
ENST00000579286.5:n.741A>C
ENST00000579886.2:c.398A>C ENSP00000463246.1:p.Lys133Thr
ENST00000580365.1:n.291A>C
ENST00000581378.5:n.278A>C
ENST00000581562.5:n.525-332A>C
ENST00000582166.1:n.541A>C
ENST00000583312.5:c.560A>C ENSP00000467920.1:p.Lys187Thr
ENST00000583760.1:n.342A>C
NM_000018.3:c.560A>C NP_000009.1:p.Lys187Thr
NM_001033859.2:c.494A>C NP_001029031.1:p.Lys165Thr
NM_001270447.1:c.629A>C NP_001257376.1:p.Lys210Thr
NM_001270448.1:c.332A>C NP_001257377.1:p.Lys111Thr
XM_006721516.2:c.560A>C XP_006721579.2:p.Lys187Thr
XM_011523829.1:c.560A>C XP_011522131.1:p.Lys187Thr
XM_011523830.1:c.560A>C XP_011522132.1:p.Lys187Thr
XR_934021.1:n.667A>C
XR_934022.1:n.667A>C
XR_934023.1:n.667A>C
XM_006721516.3:c.560A>C XP_006721579.2:p.Lys187Thr
XM_011523829.2:c.560A>C XP_011522131.1:p.Lys187Thr
XM_011523830.2:c.560A>C XP_011522132.1:p.Lys187Thr
XM_024450741.1:c.560A>C XP_024306509.1:p.Lys187Thr
XR_934021.2:n.619A>C
XR_934022.2:n.619A>C
XR_934023.2:n.619A>C
NM_000018.4:c.560A>C MANE Select NP_000009.1:p.Lys187Thr
NM_001033859.3:c.494A>C NP_001029031.1:p.Lys165Thr
NM_001270447.2:c.629A>C NP_001257376.1:p.Lys210Thr
NM_001270448.2:c.332A>C NP_001257377.1:p.Lys111Thr