Canonical Allele Identifier: CA2245709722
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222801A= , CM000679.2:g.7222801A= GRCh38
NC_000017.10:g.7126120A= , CM000679.1:g.7126120A= GRCh37
NC_000017.9:g.7066844A= NCBI36
NG_007975.1:g.7968A=
NG_008391.2:g.2250T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1013A= MANE Select ENSP00000349297.5:p.Asn338=
ENST00000322910.9:c.*968A= ENSP00000325395.5:n.*968A=
ENST00000350303.9:c.947A= ENSP00000344152.5:p.Asn316=
ENST00000356839.9:c.1013A= ENSP00000349297.5:p.Asn338=
ENST00000543245.6:c.1082A= ENSP00000438689.2:p.Asn361=
ENST00000578824.5:n.162A=
ENST00000581378.5:c.731A=
ENST00000582379.1:n.397A=
ENST00000583858.5:c.42A=
NM_000018.3:c.1013A= NP_000009.1:p.Asn338=
NM_001033859.2:c.947A= NP_001029031.1:p.Asn316=
NM_001270447.1:c.1082A= NP_001257376.1:p.Asn361=
NM_001270448.1:c.785A= NP_001257377.1:p.Asn262=
XM_006721516.2:c.1013A= XP_006721579.2:p.Asn338=
XM_011523829.1:c.1013A= XP_011522131.1:p.Asn338=
XM_011523830.1:c.1013A= XP_011522132.1:p.Asn338=
XR_934021.1:n.1120A=
XR_934022.1:n.1120A=
XR_934023.1:n.1120A=
XM_006721516.3:c.1013A= XP_006721579.2:p.Asn338=
XM_011523829.2:c.1013A= XP_011522131.1:p.Asn338=
XM_011523830.2:c.1013A= XP_011522132.1:p.Asn338=
XM_024450741.1:c.1013A= XP_024306509.1:p.Asn338=
XR_934021.2:n.1072A=
XR_934022.2:n.1072A=
XR_934023.2:n.1072A=
NM_000018.4:c.1013A= MANE Select NP_000009.1:p.Asn338=
NM_001033859.3:c.947A= NP_001029031.1:p.Asn316=
NM_001270447.2:c.1082A= NP_001257376.1:p.Asn361=
NM_001270448.2:c.785A= NP_001257377.1:p.Asn262=