Canonical Allele Identifier: CA397725556
Gene: ACADVL HGNC NCBI

Linked Data

gnomAD v4: 17-7224519-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224519G>C , CM000679.2:g.7224519G>C GRCh38
NC_000017.10:g.7127838G>C , CM000679.1:g.7127838G>C GRCh37
NC_000017.9:g.7068562G>C NCBI36
NG_007975.1:g.9686G>C
NG_008391.2:g.532C>G
NG_033038.1:g.15026C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1645G>C MANE Select ENSP00000349297.5:p.Ala549Pro
ENST00000322910.9:c.*1600G>C ENSP00000325395.5:n.*1600G>C
ENST00000350303.9:c.1579G>C ENSP00000344152.5:p.Ala527Pro
ENST00000356839.9:c.1645G>C ENSP00000349297.5:p.Ala549Pro
ENST00000542255.6:c.503G>C
ENST00000543245.6:c.1714G>C ENSP00000438689.2:p.Ala572Pro
ENST00000578319.5:n.226G>C
ENST00000578711.1:n.1015G>C
ENST00000578809.5:n.217G>C
ENST00000579391.1:n.249G>C
ENST00000579425.5:n.761G>C
ENST00000579546.1:c.380G>C
ENST00000582450.1:n.153G>C
ENST00000583074.5:n.266G>C
ENST00000583848.5:c.31G>C ENSP00000466487.1:p.Ala11Pro
ENST00000583850.5:n.416G>C
ENST00000583858.5:c.576G>C
ENST00000585203.6:n.836G>C
NM_000018.3:c.1645G>C NP_000009.1:p.Ala549Pro
NM_001033859.2:c.1579G>C NP_001029031.1:p.Ala527Pro
NM_001270447.1:c.1714G>C NP_001257376.1:p.Ala572Pro
NM_001270448.1:c.1417G>C NP_001257377.1:p.Ala473Pro
XM_006721516.2:c.1645G>C XP_006721579.2:p.Ala549Pro
XM_011523829.1:c.1543G>C XP_011522131.1:p.Ala515Pro
XM_011523830.1:c.1543G>C XP_011522132.1:p.Ala515Pro
XR_934021.1:n.1748G>C
XR_934022.1:n.1654G>C
XR_934023.1:n.1654G>C
XM_006721516.3:c.1645G>C XP_006721579.2:p.Ala549Pro
XM_011523829.2:c.1543G>C XP_011522131.1:p.Ala515Pro
XM_011523830.2:c.1543G>C XP_011522132.1:p.Ala515Pro
XM_024450741.1:c.1633G>C XP_024306509.1:p.Ala545Pro
XR_934021.2:n.1700G>C
XR_934022.2:n.1606G>C
XR_934023.2:n.1606G>C
NM_000018.4:c.1645G>C MANE Select NP_000009.1:p.Ala549Pro
NM_001033859.3:c.1579G>C NP_001029031.1:p.Ala527Pro
NM_001270447.2:c.1714G>C NP_001257376.1:p.Ala572Pro
NM_001270448.2:c.1417G>C NP_001257377.1:p.Ala473Pro