Canonical Allele Identifier: CA2245699964
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221521T= , CM000679.2:g.7221521T= GRCh38
NC_000017.10:g.7124840T= , CM000679.1:g.7124840T= GRCh37
NC_000017.9:g.7065564T= NCBI36
NG_007975.1:g.6688T=
NG_008391.2:g.3530A=

Transcript Alleles

HGVS Amino-acid change
ENST00000356839.10:c.478-17T= MANE Select ENSP00000349297.5:p.=
ENST00000322910.9:c.*433-17T= ENSP00000325395.5:p.=
ENST00000350303.9:c.412-17T= ENSP00000344152.5:p.=
ENST00000356839.9:c.478-17T= ENSP00000349297.5:p.=
ENST00000543245.6:c.547-17T= ENSP00000438689.2:p.=
ENST00000577191.5:n.555-17T=
ENST00000577433.5:n.686-17T=
ENST00000577857.5:n.294-17T=
ENST00000579286.5:n.659-17T=
ENST00000579886.2:c.316-17T= ENSP00000463246.1:p.=
ENST00000580365.1:n.209-17T=
ENST00000581378.5:n.179T=
ENST00000581562.5:n.525-431T=
ENST00000582166.1:n.459-17T=
ENST00000583312.5:c.478-17T= ENSP00000467920.1:p.=
ENST00000583760.1:n.243T=
NM_000018.3:c.478-17T= NP_000009.1:p.=
NM_001033859.2:c.412-17T= NP_001029031.1:p.=
NM_001270447.1:c.547-17T= NP_001257376.1:p.=
NM_001270448.1:c.250-17T= NP_001257377.1:p.=
XM_006721516.2:c.478-17T= XP_006721579.2:p.=
XM_011523829.1:c.478-17T= XP_011522131.1:p.=
XM_011523830.1:c.478-17T= XP_011522132.1:p.=
XR_934021.1:n.585-17T=
XR_934022.1:n.585-17T=
XR_934023.1:n.585-17T=
XM_006721516.3:c.478-17T= XP_006721579.2:p.=
XM_011523829.2:c.478-17T= XP_011522131.1:p.=
XM_011523830.2:c.478-17T= XP_011522132.1:p.=
XM_024450741.1:c.478-17T= XP_024306509.1:p.=
XR_934021.2:n.537-17T=
XR_934022.2:n.537-17T=
XR_934023.2:n.537-17T=
NM_000018.4:c.478-17T= MANE Select NP_000009.1:p.=
NM_001033859.3:c.412-17T= NP_001029031.1:p.=
NM_001270447.2:c.547-17T= NP_001257376.1:p.=
NM_001270448.2:c.250-17T= NP_001257377.1:p.=