Canonical Allele Identifier: CA2245709428
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222736G= , CM000679.2:g.7222736G= GRCh38
NC_000017.10:g.7126055G= , CM000679.1:g.7126055G= GRCh37
NC_000017.9:g.7066779G= NCBI36
NG_007975.1:g.7903G=
NG_008391.2:g.2315C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.948G= MANE Select ENSP00000349297.5:p.Arg316=
ENST00000322910.9:c.*903G= ENSP00000325395.5:n.*903G=
ENST00000350303.9:c.882G= ENSP00000344152.5:p.Arg294=
ENST00000356839.9:c.948G= ENSP00000349297.5:p.Arg316=
ENST00000543245.6:c.1017G= ENSP00000438689.2:p.Arg339=
ENST00000578824.5:n.97G=
ENST00000581378.5:c.666G=
ENST00000582379.1:n.332G=
NM_000018.3:c.948G= NP_000009.1:p.Arg316=
NM_001033859.2:c.882G= NP_001029031.1:p.Arg294=
NM_001270447.1:c.1017G= NP_001257376.1:p.Arg339=
NM_001270448.1:c.720G= NP_001257377.1:p.Arg240=
XM_006721516.2:c.948G= XP_006721579.2:p.Arg316=
XM_011523829.1:c.948G= XP_011522131.1:p.Arg316=
XM_011523830.1:c.948G= XP_011522132.1:p.Arg316=
XR_934021.1:n.1055G=
XR_934022.1:n.1055G=
XR_934023.1:n.1055G=
XM_006721516.3:c.948G= XP_006721579.2:p.Arg316=
XM_011523829.2:c.948G= XP_011522131.1:p.Arg316=
XM_011523830.2:c.948G= XP_011522132.1:p.Arg316=
XM_024450741.1:c.948G= XP_024306509.1:p.Arg316=
XR_934021.2:n.1007G=
XR_934022.2:n.1007G=
XR_934023.2:n.1007G=
NM_000018.4:c.948G= MANE Select NP_000009.1:p.Arg316=
NM_001033859.3:c.882G= NP_001029031.1:p.Arg294=
NM_001270447.2:c.1017G= NP_001257376.1:p.Arg339=
NM_001270448.2:c.720G= NP_001257377.1:p.Arg240=