Canonical Allele Identifier: CA2245709997
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222864C= , CM000679.2:g.7222864C= GRCh38
NC_000017.10:g.7126183C= , CM000679.1:g.7126183C= GRCh37
NC_000017.9:g.7066907C= NCBI36
NG_007975.1:g.8031C=
NG_008391.2:g.2187G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1076C= MANE Select ENSP00000349297.5:p.Ala359=
ENST00000322910.9:c.*1031C= ENSP00000325395.5:n.*1031C=
ENST00000350303.9:c.1010C= ENSP00000344152.5:p.Ala337=
ENST00000356839.9:c.1076C= ENSP00000349297.5:p.Ala359=
ENST00000543245.6:c.1145C= ENSP00000438689.2:p.Ala382=
ENST00000578824.5:n.225C=
ENST00000582379.1:n.460C=
ENST00000583858.5:c.105C=
ENST00000585203.6:n.17C=
NM_000018.3:c.1076C= NP_000009.1:p.Ala359=
NM_001033859.2:c.1010C= NP_001029031.1:p.Ala337=
NM_001270447.1:c.1145C= NP_001257376.1:p.Ala382=
NM_001270448.1:c.848C= NP_001257377.1:p.Ala283=
XM_006721516.2:c.1076C= XP_006721579.2:p.Ala359=
XM_011523829.1:c.1076C= XP_011522131.1:p.Ala359=
XM_011523830.1:c.1076C= XP_011522132.1:p.Ala359=
XR_934021.1:n.1183C=
XR_934022.1:n.1183C=
XR_934023.1:n.1183C=
XM_006721516.3:c.1076C= XP_006721579.2:p.Ala359=
XM_011523829.2:c.1076C= XP_011522131.1:p.Ala359=
XM_011523830.2:c.1076C= XP_011522132.1:p.Ala359=
XM_024450741.1:c.1076C= XP_024306509.1:p.Ala359=
XR_934021.2:n.1135C=
XR_934022.2:n.1135C=
XR_934023.2:n.1135C=
NM_000018.4:c.1076C= MANE Select NP_000009.1:p.Ala359=
NM_001033859.3:c.1010C= NP_001029031.1:p.Ala337=
NM_001270447.2:c.1145C= NP_001257376.1:p.Ala382=
NM_001270448.2:c.848C= NP_001257377.1:p.Ala283=