Canonical Allele Identifier: CA2245700361
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221645G= , CM000679.2:g.7221645G= GRCh38
NC_000017.10:g.7124964G= , CM000679.1:g.7124964G= GRCh37
NC_000017.9:g.7065688G= NCBI36
NG_007975.1:g.6812G=
NG_008391.2:g.3406C=

Transcript Alleles

HGVS Amino-acid change
ENST00000356839.10:c.585G= MANE Select ENSP00000349297.5:p.Lys195=
ENST00000322910.9:c.*540G= ENSP00000325395.5:n.*540G=
ENST00000350303.9:c.519G= ENSP00000344152.5:p.Lys173=
ENST00000356839.9:c.585G= ENSP00000349297.5:p.Lys195=
ENST00000543245.6:c.654G= ENSP00000438689.2:p.Lys218=
ENST00000577191.5:n.662G=
ENST00000577433.5:n.793G=
ENST00000577857.5:n.401G=
ENST00000579286.5:n.766G=
ENST00000579886.2:c.423G= ENSP00000463246.1:p.Lys141=
ENST00000580365.1:n.316G=
ENST00000581378.5:c.303G=
ENST00000581562.5:n.525-307G=
ENST00000583312.5:c.585G= ENSP00000467920.1:p.Lys195=
ENST00000583760.1:n.367G=
NM_000018.3:c.585G= NP_000009.1:p.Lys195=
NM_001033859.2:c.519G= NP_001029031.1:p.Lys173=
NM_001270447.1:c.654G= NP_001257376.1:p.Lys218=
NM_001270448.1:c.357G= NP_001257377.1:p.Lys119=
XM_006721516.2:c.585G= XP_006721579.2:p.Lys195=
XM_011523829.1:c.585G= XP_011522131.1:p.Lys195=
XM_011523830.1:c.585G= XP_011522132.1:p.Lys195=
XR_934021.1:n.692G=
XR_934022.1:n.692G=
XR_934023.1:n.692G=
XM_006721516.3:c.585G= XP_006721579.2:p.Lys195=
XM_011523829.2:c.585G= XP_011522131.1:p.Lys195=
XM_011523830.2:c.585G= XP_011522132.1:p.Lys195=
XM_024450741.1:c.585G= XP_024306509.1:p.Lys195=
XR_934021.2:n.644G=
XR_934022.2:n.644G=
XR_934023.2:n.644G=
NM_000018.4:c.585G= MANE Select NP_000009.1:p.Lys195=
NM_001033859.3:c.519G= NP_001029031.1:p.Lys173=
NM_001270447.2:c.654G= NP_001257376.1:p.Lys218=
NM_001270448.2:c.357G= NP_001257377.1:p.Lys119=