Canonical Allele Identifier: CA2245700012
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221542C= , CM000679.2:g.7221542C= GRCh38
NC_000017.10:g.7124861C= , CM000679.1:g.7124861C= GRCh37
NC_000017.9:g.7065585C= NCBI36
NG_007975.1:g.6709C=
NG_008391.2:g.3509G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.482C= MANE Select ENSP00000349297.5:p.Ala161=
ENST00000322910.9:c.*437C= ENSP00000325395.5:n.*437C=
ENST00000350303.9:c.416C= ENSP00000344152.5:p.Ala139=
ENST00000356839.9:c.482C= ENSP00000349297.5:p.Ala161=
ENST00000543245.6:c.551C= ENSP00000438689.2:p.Ala184=
ENST00000577191.5:n.559C=
ENST00000577433.5:n.690C=
ENST00000577857.5:n.298C=
ENST00000579286.5:n.663C=
ENST00000579886.2:c.320C= ENSP00000463246.1:p.Ala107=
ENST00000580365.1:n.213C=
ENST00000581378.5:c.200C=
ENST00000581562.5:n.525-410C=
ENST00000582166.1:n.463C=
ENST00000583312.5:c.482C= ENSP00000467920.1:p.Ala161=
ENST00000583760.1:n.264C=
NM_000018.3:c.482C= NP_000009.1:p.Ala161=
NM_001033859.2:c.416C= NP_001029031.1:p.Ala139=
NM_001270447.1:c.551C= NP_001257376.1:p.Ala184=
NM_001270448.1:c.254C= NP_001257377.1:p.Ala85=
XM_006721516.2:c.482C= XP_006721579.2:p.Ala161=
XM_011523829.1:c.482C= XP_011522131.1:p.Ala161=
XM_011523830.1:c.482C= XP_011522132.1:p.Ala161=
XR_934021.1:n.589C=
XR_934022.1:n.589C=
XR_934023.1:n.589C=
XM_006721516.3:c.482C= XP_006721579.2:p.Ala161=
XM_011523829.2:c.482C= XP_011522131.1:p.Ala161=
XM_011523830.2:c.482C= XP_011522132.1:p.Ala161=
XM_024450741.1:c.482C= XP_024306509.1:p.Ala161=
XR_934021.2:n.541C=
XR_934022.2:n.541C=
XR_934023.2:n.541C=
NM_000018.4:c.482C= MANE Select NP_000009.1:p.Ala161=
NM_001033859.3:c.416C= NP_001029031.1:p.Ala139=
NM_001270447.2:c.551C= NP_001257376.1:p.Ala184=
NM_001270448.2:c.254C= NP_001257377.1:p.Ala85=