Canonical Allele Identifier: CA2245711476
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7223660T= , CM000679.2:g.7223660T= GRCh38
NC_000017.10:g.7126979T= , CM000679.1:g.7126979T= GRCh37
NC_000017.9:g.7067703T= NCBI36
NG_007975.1:g.8827T=
NG_008391.2:g.1391A=
NG_033038.1:g.15885A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1199T= MANE Select ENSP00000349297.5:p.Val400=
ENST00000322910.9:c.*1154T= ENSP00000325395.5:n.*1154T=
ENST00000350303.9:c.1133T= ENSP00000344152.5:p.Val378=
ENST00000356839.9:c.1199T= ENSP00000349297.5:p.Val400=
ENST00000542255.6:c.57T=
ENST00000543245.6:c.1268T= ENSP00000438689.2:p.Val423=
ENST00000578579.2:n.370T=
ENST00000578711.1:n.156T=
ENST00000578824.5:n.615T=
ENST00000579425.5:n.223T=
ENST00000579546.1:c.36T=
ENST00000583858.5:c.228T=
ENST00000585203.6:n.407T=
NM_000018.3:c.1199T= NP_000009.1:p.Val400=
NM_001033859.2:c.1133T= NP_001029031.1:p.Val378=
NM_001270447.1:c.1268T= NP_001257376.1:p.Val423=
NM_001270448.1:c.971T= NP_001257377.1:p.Val324=
XM_006721516.2:c.1199T= XP_006721579.2:p.Val400=
XM_011523829.1:c.1199T= XP_011522131.1:p.Val400=
XM_011523830.1:c.1199T= XP_011522132.1:p.Val400=
XR_934021.1:n.1306T=
XR_934022.1:n.1306T=
XR_934023.1:n.1306T=
XM_006721516.3:c.1199T= XP_006721579.2:p.Val400=
XM_011523829.2:c.1199T= XP_011522131.1:p.Val400=
XM_011523830.2:c.1199T= XP_011522132.1:p.Val400=
XM_024450741.1:c.1199T= XP_024306509.1:p.Val400=
XR_934021.2:n.1258T=
XR_934022.2:n.1258T=
XR_934023.2:n.1258T=
NM_000018.4:c.1199T= MANE Select NP_000009.1:p.Val400=
NM_001033859.3:c.1133T= NP_001029031.1:p.Val378=
NM_001270447.2:c.1268T= NP_001257376.1:p.Val423=
NM_001270448.2:c.971T= NP_001257377.1:p.Val324=