Canonical Allele Identifier: CA2245709563
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222764G= , CM000679.2:g.7222764G= GRCh38
NC_000017.10:g.7126083G= , CM000679.1:g.7126083G= GRCh37
NC_000017.9:g.7066807G= NCBI36
NG_007975.1:g.7931G=
NG_008391.2:g.2287C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.976G= MANE Select ENSP00000349297.5:p.Val326=
ENST00000322910.9:c.*931G= ENSP00000325395.5:n.*931G=
ENST00000350303.9:c.910G= ENSP00000344152.5:p.Val304=
ENST00000356839.9:c.976G= ENSP00000349297.5:p.Val326=
ENST00000543245.6:c.1045G= ENSP00000438689.2:p.Val349=
ENST00000578824.5:n.125G=
ENST00000581378.5:c.694G=
ENST00000582379.1:n.360G=
ENST00000583858.5:c.5G=
NM_000018.3:c.976G= NP_000009.1:p.Val326=
NM_001033859.2:c.910G= NP_001029031.1:p.Val304=
NM_001270447.1:c.1045G= NP_001257376.1:p.Val349=
NM_001270448.1:c.748G= NP_001257377.1:p.Val250=
XM_006721516.2:c.976G= XP_006721579.2:p.Val326=
XM_011523829.1:c.976G= XP_011522131.1:p.Val326=
XM_011523830.1:c.976G= XP_011522132.1:p.Val326=
XR_934021.1:n.1083G=
XR_934022.1:n.1083G=
XR_934023.1:n.1083G=
XM_006721516.3:c.976G= XP_006721579.2:p.Val326=
XM_011523829.2:c.976G= XP_011522131.1:p.Val326=
XM_011523830.2:c.976G= XP_011522132.1:p.Val326=
XM_024450741.1:c.976G= XP_024306509.1:p.Val326=
XR_934021.2:n.1035G=
XR_934022.2:n.1035G=
XR_934023.2:n.1035G=
NM_000018.4:c.976G= MANE Select NP_000009.1:p.Val326=
NM_001033859.3:c.910G= NP_001029031.1:p.Val304=
NM_001270447.2:c.1045G= NP_001257376.1:p.Val349=
NM_001270448.2:c.748G= NP_001257377.1:p.Val250=