Canonical Allele Identifier: CA397725683
Gene: ACADVL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224660A>C , CM000679.2:g.7224660A>C GRCh38
NC_000017.10:g.7127979A>C , CM000679.1:g.7127979A>C GRCh37
NC_000017.9:g.7068703A>C NCBI36
NG_007975.1:g.9827A>C
NG_008391.2:g.391T>G
NG_033038.1:g.14885T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1697A>C MANE Select ENSP00000349297.5:p.Gln566Pro
ENST00000322910.9:c.*1652A>C ENSP00000325395.5:n.*1652A>C
ENST00000350303.9:c.1631A>C ENSP00000344152.5:p.Gln544Pro
ENST00000356839.9:c.1697A>C ENSP00000349297.5:p.Gln566Pro
ENST00000542255.6:c.537-55A>C
ENST00000543245.6:c.1766A>C ENSP00000438689.2:p.Gln589Pro
ENST00000578033.1:n.28A>C
ENST00000578319.5:n.278A>C
ENST00000578711.1:n.1156A>C
ENST00000578809.5:n.269A>C
ENST00000579425.5:n.813A>C
ENST00000579546.1:c.432A>C
ENST00000582450.1:n.294A>C
ENST00000583074.5:n.300-55A>C
ENST00000583848.5:c.65-2A>C ENSP00000466487.1:n.65-2A>C
ENST00000583850.5:n.468A>C
ENST00000583858.5:c.628A>C
ENST00000585203.6:n.888A>C
NM_000018.3:c.1697A>C NP_000009.1:p.Gln566Pro
NM_001033859.2:c.1631A>C NP_001029031.1:p.Gln544Pro
NM_001270447.1:c.1766A>C NP_001257376.1:p.Gln589Pro
NM_001270448.1:c.1469A>C NP_001257377.1:p.Gln490Pro
XM_006721516.2:c.1679-55A>C XP_006721579.2:n.1679-55A>C
XM_011523829.1:c.1577-55A>C XP_011522131.1:n.1577-55A>C
XM_011523830.1:c.1595A>C XP_011522132.1:p.Gln532Pro
XR_934021.1:n.1800A>C
XR_934022.1:n.1706A>C
XR_934023.1:n.1688-55A>C
XM_006721516.3:c.1679-55A>C XP_006721579.2:n.1679-55A>C
XM_011523829.2:c.1577-55A>C XP_011522131.1:n.1577-55A>C
XM_011523830.2:c.1595A>C XP_011522132.1:p.Gln532Pro
XM_024450741.1:c.1685A>C XP_024306509.1:p.Gln562Pro
XR_934021.2:n.1752A>C
XR_934022.2:n.1658A>C
XR_934023.2:n.1640-55A>C
NM_000018.4:c.1697A>C MANE Select NP_000009.1:p.Gln566Pro
NM_001033859.3:c.1631A>C NP_001029031.1:p.Gln544Pro
NM_001270447.2:c.1766A>C NP_001257376.1:p.Gln589Pro
NM_001270448.2:c.1469A>C NP_001257377.1:p.Gln490Pro