Canonical Allele Identifier: CA2245710607
Community Standard Title: NM_000018.4(ACADVL):c.1144A= (p.Lys382=)
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7223199A= , CM000679.2:g.7223199A= GRCh38
NC_000017.10:g.7126518A= , CM000679.1:g.7126518A= GRCh37
NC_000017.9:g.7067242A= NCBI36
NG_007975.1:g.8366A=
NG_008391.2:g.1852T=

Transcript Alleles

HGVS Amino-acid Change
NM_000018.4:c.1144A= MANE Select NP_000009.1:p.Lys382=
ENST00000356839.10:c.1144A= MANE Select ENSP00000349297.5:p.Lys382=
NM_000018.3:c.1144A= NP_000009.1:p.Lys382=
NM_001033859.2:c.1078A= NP_001029031.1:p.Lys360=
NM_001033859.3:c.1078A= NP_001029031.1:p.Lys360=
NM_001270447.1:c.1213A= NP_001257376.1:p.Lys405=
NM_001270447.2:c.1213A= NP_001257376.1:p.Lys405=
NM_001270448.1:c.916A= NP_001257377.1:p.Lys306=
NM_001270448.2:c.916A= NP_001257377.1:p.Lys306=
ENST00000322910.9:c.*1099A= ENSP00000325395.5:n.*1099A=
ENST00000350303.9:c.1078A= ENSP00000344152.5:p.Lys360=
ENST00000356839.9:c.1144A= ENSP00000349297.5:p.Lys382=
ENST00000542255.6:c.2A=
ENST00000543245.6:c.1213A= ENSP00000438689.2:p.Lys405=
ENST00000578579.2:n.93A=
ENST00000578824.5:n.560A=
ENST00000579425.5:n.168A=
ENST00000582379.1:n.795A=
ENST00000583858.5:c.173A=
ENST00000585203.6:n.352A=
XM_006721516.2:c.1144A= XP_006721579.2:p.Lys382=
XM_006721516.3:c.1144A= XP_006721579.2:p.Lys382=
XM_011523829.1:c.1144A= XP_011522131.1:p.Lys382=
XM_011523829.2:c.1144A= XP_011522131.1:p.Lys382=
XM_011523830.1:c.1144A= XP_011522132.1:p.Lys382=
XM_011523830.2:c.1144A= XP_011522132.1:p.Lys382=
XM_024450741.1:c.1144A= XP_024306509.1:p.Lys382=
XR_934021.1:n.1251A=
XR_934021.2:n.1203A=
XR_934022.1:n.1251A=
XR_934022.2:n.1203A=
XR_934023.1:n.1251A=
XR_934023.2:n.1203A=