Canonical Allele Identifier: CA2635784382

Gene: ACADVL

Linked Data

• gnomAD v4: 17-7224439-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7224439C>A , CM000679.2:g.7224439C>A	GRCh38
NC_000017.10:g.7127758C>A , CM000679.1:g.7127758C>A	GRCh37
NC_000017.9:g.7068482C>A	NCBI36
NG_007975.1:g.9606C>A
NG_008391.2:g.612G>T
NG_033038.1:g.15106G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000356839.10:c.1606-41C>A MANE Select	ENSP00000349297.5:n.1606-41C>A
ENST00000322910.9:c.*1561-41C>A	ENSP00000325395.5:n.*1561-41C>A
ENST00000350303.9:c.1540-41C>A	ENSP00000344152.5:n.1540-41C>A
ENST00000356839.9:c.1606-41C>A	ENSP00000349297.5:n.1606-41C>A
ENST00000542255.6:c.464-41C>A
ENST00000543245.6:c.1675-41C>A	ENSP00000438689.2:n.1675-41C>A
ENST00000578319.5:n.146C>A
ENST00000578711.1:n.935C>A
ENST00000578809.5:n.178-41C>A
ENST00000579391.1:n.214-45C>A
ENST00000579425.5:n.722-41C>A
ENST00000579546.1:c.345-45C>A
ENST00000579894.5:n.393-41C>A
ENST00000582450.1:n.114-41C>A
ENST00000583074.5:n.227-41C>A
ENST00000583850.5:n.381-45C>A
ENST00000583858.5:c.537-41C>A
ENST00000585203.6:n.797-41C>A
NM_000018.3:c.1606-41C>A	NP_000009.1:n.1606-41C>A
NM_001033859.2:c.1540-41C>A	NP_001029031.1:n.1540-41C>A
NM_001270447.1:c.1675-41C>A	NP_001257376.1:n.1675-41C>A
NM_001270448.1:c.1378-41C>A	NP_001257377.1:n.1378-41C>A
XM_006721516.2:c.1606-41C>A	XP_006721579.2:n.1606-41C>A
XM_011523829.1:c.1508-45C>A	XP_011522131.1:n.1508-45C>A
XM_011523830.1:c.1508-45C>A	XP_011522132.1:n.1508-45C>A
XR_934021.1:n.1713-45C>A
XR_934022.1:n.1615-41C>A
XR_934023.1:n.1615-41C>A
XM_006721516.3:c.1606-41C>A	XP_006721579.2:n.1606-41C>A
XM_011523829.2:c.1508-45C>A	XP_011522131.1:n.1508-45C>A
XM_011523830.2:c.1508-45C>A	XP_011522132.1:n.1508-45C>A
XM_024450741.1:c.1553C>A	XP_024306509.1:p.Pro518Gln
XR_934021.2:n.1665-45C>A
XR_934022.2:n.1567-41C>A
XR_934023.2:n.1567-41C>A
NM_000018.4:c.1606-41C>A MANE Select	NP_000009.1:n.1606-41C>A
NM_001033859.3:c.1540-41C>A	NP_001029031.1:n.1540-41C>A
NM_001270447.2:c.1675-41C>A	NP_001257376.1:n.1675-41C>A
NM_001270448.2:c.1378-41C>A	NP_001257377.1:n.1378-41C>A