Canonical Allele Identifier: CA397723621
Gene: ACADVL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222179A>C , CM000679.2:g.7222179A>C GRCh38
NC_000017.10:g.7125498A>C , CM000679.1:g.7125498A>C GRCh37
NC_000017.9:g.7066222A>C NCBI36
NG_007975.1:g.7346A>C
NG_008391.2:g.2872T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.755A>C MANE Select ENSP00000349297.5:p.Asn252Thr
ENST00000322910.9:c.*710A>C ENSP00000325395.5:n.*710A>C
ENST00000350303.9:c.689A>C ENSP00000344152.5:p.Asn230Thr
ENST00000356839.9:c.755A>C ENSP00000349297.5:p.Asn252Thr
ENST00000543245.6:c.824A>C ENSP00000438689.2:p.Asn275Thr
ENST00000577191.5:n.927A>C
ENST00000581378.5:c.473A>C
ENST00000582379.1:n.139A>C
NM_000018.3:c.755A>C NP_000009.1:p.Asn252Thr
NM_001033859.2:c.689A>C NP_001029031.1:p.Asn230Thr
NM_001270447.1:c.824A>C NP_001257376.1:p.Asn275Thr
NM_001270448.1:c.527A>C NP_001257377.1:p.Asn176Thr
XM_006721516.2:c.755A>C XP_006721579.2:p.Asn252Thr
XM_011523829.1:c.755A>C XP_011522131.1:p.Asn252Thr
XM_011523830.1:c.755A>C XP_011522132.1:p.Asn252Thr
XR_934021.1:n.862A>C
XR_934022.1:n.862A>C
XR_934023.1:n.862A>C
XM_006721516.3:c.755A>C XP_006721579.2:p.Asn252Thr
XM_011523829.2:c.755A>C XP_011522131.1:p.Asn252Thr
XM_011523830.2:c.755A>C XP_011522132.1:p.Asn252Thr
XM_024450741.1:c.755A>C XP_024306509.1:p.Asn252Thr
XR_934021.2:n.814A>C
XR_934022.2:n.814A>C
XR_934023.2:n.814A>C
NM_000018.4:c.755A>C MANE Select NP_000009.1:p.Asn252Thr
NM_001033859.3:c.689A>C NP_001029031.1:p.Asn230Thr
NM_001270447.2:c.824A>C NP_001257376.1:p.Asn275Thr
NM_001270448.2:c.527A>C NP_001257377.1:p.Asn176Thr