Canonical Allele Identifier: CA2245708908
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222561T= , CM000679.2:g.7222561T= GRCh38
NC_000017.10:g.7125880T= , CM000679.1:g.7125880T= GRCh37
NC_000017.9:g.7066604T= NCBI36
NG_007975.1:g.7728T=
NG_008391.2:g.2490A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.879-106T= MANE Select ENSP00000349297.5:n.879-106T=
ENST00000322910.9:c.*834-106T= ENSP00000325395.5:n.*834-106T=
ENST00000350303.9:c.813-106T= ENSP00000344152.5:n.813-106T=
ENST00000356839.9:c.879-106T= ENSP00000349297.5:n.879-106T=
ENST00000543245.6:c.948-106T= ENSP00000438689.2:n.948-106T=
ENST00000581378.5:c.597-106T=
ENST00000582379.1:n.263-106T=
NM_000018.3:c.879-106T= NP_000009.1:n.879-106T=
NM_001033859.2:c.813-106T= NP_001029031.1:n.813-106T=
NM_001270447.1:c.948-106T= NP_001257376.1:n.948-106T=
NM_001270448.1:c.651-106T= NP_001257377.1:n.651-106T=
XM_006721516.2:c.879-106T= XP_006721579.2:n.879-106T=
XM_011523829.1:c.879-106T= XP_011522131.1:n.879-106T=
XM_011523830.1:c.879-106T= XP_011522132.1:n.879-106T=
XR_934021.1:n.986-106T=
XR_934022.1:n.986-106T=
XR_934023.1:n.986-106T=
XM_006721516.3:c.879-106T= XP_006721579.2:n.879-106T=
XM_011523829.2:c.879-106T= XP_011522131.1:n.879-106T=
XM_011523830.2:c.879-106T= XP_011522132.1:n.879-106T=
XM_024450741.1:c.879-106T= XP_024306509.1:n.879-106T=
XR_934021.2:n.938-106T=
XR_934022.2:n.938-106T=
XR_934023.2:n.938-106T=
NM_000018.4:c.879-106T= MANE Select NP_000009.1:n.879-106T=
NM_001033859.3:c.813-106T= NP_001029031.1:n.813-106T=
NM_001270447.2:c.948-106T= NP_001257376.1:n.948-106T=
NM_001270448.2:c.651-106T= NP_001257377.1:n.651-106T=