Canonical Allele Identifier: CA2245699944
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221516C= , CM000679.2:g.7221516C= GRCh38
NC_000017.10:g.7124835C= , CM000679.1:g.7124835C= GRCh37
NC_000017.9:g.7065559C= NCBI36
NG_007975.1:g.6683C=
NG_008391.2:g.3535G=

Transcript Alleles

HGVS Amino-acid change
ENST00000356839.10:c.478-22C= MANE Select ENSP00000349297.5:n.478-22C=
ENST00000322910.9:c.*433-22C= ENSP00000325395.5:n.*433-22C=
ENST00000350303.9:c.412-22C= ENSP00000344152.5:n.412-22C=
ENST00000356839.9:c.478-22C= ENSP00000349297.5:n.478-22C=
ENST00000543245.6:c.547-22C= ENSP00000438689.2:n.547-22C=
ENST00000577191.5:n.555-22C=
ENST00000577433.5:n.686-22C=
ENST00000577857.5:n.294-22C=
ENST00000579286.5:n.659-22C=
ENST00000579886.2:c.316-22C= ENSP00000463246.1:n.316-22C=
ENST00000580365.1:n.209-22C=
ENST00000581378.5:c.177-3C=
ENST00000581562.5:n.525-436C=
ENST00000582166.1:n.459-22C=
ENST00000583312.5:c.478-22C= ENSP00000467920.1:n.478-22C=
ENST00000583760.1:n.238C=
NM_000018.3:c.478-22C= NP_000009.1:n.478-22C=
NM_001033859.2:c.412-22C= NP_001029031.1:n.412-22C=
NM_001270447.1:c.547-22C= NP_001257376.1:n.547-22C=
NM_001270448.1:c.250-22C= NP_001257377.1:n.250-22C=
XM_006721516.2:c.478-22C= XP_006721579.2:n.478-22C=
XM_011523829.1:c.478-22C= XP_011522131.1:n.478-22C=
XM_011523830.1:c.478-22C= XP_011522132.1:n.478-22C=
XR_934021.1:n.585-22C=
XR_934022.1:n.585-22C=
XR_934023.1:n.585-22C=
XM_006721516.3:c.478-22C= XP_006721579.2:n.478-22C=
XM_011523829.2:c.478-22C= XP_011522131.1:n.478-22C=
XM_011523830.2:c.478-22C= XP_011522132.1:n.478-22C=
XM_024450741.1:c.478-22C= XP_024306509.1:n.478-22C=
XR_934021.2:n.537-22C=
XR_934022.2:n.537-22C=
XR_934023.2:n.537-22C=
NM_000018.4:c.478-22C= MANE Select NP_000009.1:n.478-22C=
NM_001033859.3:c.412-22C= NP_001029031.1:n.412-22C=
NM_001270447.2:c.547-22C= NP_001257376.1:n.547-22C=
NM_001270448.2:c.250-22C= NP_001257377.1:n.250-22C=