Canonical Allele Identifier: CA2635784737

Gene: ACADVL

Linked Data

• gnomAD v4: 17-7224591-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7224591C>A , CM000679.2:g.7224591C>A	GRCh38
NC_000017.10:g.7127910C>A , CM000679.1:g.7127910C>A	GRCh37
NC_000017.9:g.7068634C>A	NCBI36
NG_007975.1:g.9758C>A
NG_008391.2:g.460G>T
NG_033038.1:g.14954G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000356839.10:c.1678+39C>A MANE Select	ENSP00000349297.5:n.1678+39C>A
ENST00000322910.9:c.*1633+39C>A	ENSP00000325395.5:n.*1633+39C>A
ENST00000350303.9:c.1612+39C>A	ENSP00000344152.5:n.1612+39C>A
ENST00000356839.9:c.1678+39C>A	ENSP00000349297.5:n.1678+39C>A
ENST00000542255.6:c.536+39C>A
ENST00000543245.6:c.1747+39C>A	ENSP00000438689.2:n.1747+39C>A
ENST00000578319.5:n.259+39C>A
ENST00000578711.1:n.1087C>A
ENST00000578809.5:n.250+39C>A
ENST00000579391.1:n.321C>A
ENST00000579425.5:n.794+39C>A
ENST00000579546.1:c.413+39C>A
ENST00000582450.1:n.225C>A
ENST00000583074.5:n.299+39C>A
ENST00000583848.5:c.64+39C>A	ENSP00000466487.1:n.64+39C>A
ENST00000583850.5:n.449+39C>A
ENST00000583858.5:c.609+39C>A
ENST00000585203.6:n.869+39C>A
NM_000018.3:c.1678+39C>A	NP_000009.1:n.1678+39C>A
NM_001033859.2:c.1612+39C>A	NP_001029031.1:n.1612+39C>A
NM_001270447.1:c.1747+39C>A	NP_001257376.1:n.1747+39C>A
NM_001270448.1:c.1450+39C>A	NP_001257377.1:n.1450+39C>A
XM_006721516.2:c.1678+39C>A	XP_006721579.2:n.1678+39C>A
XM_011523829.1:c.1576+39C>A	XP_011522131.1:n.1576+39C>A
XM_011523830.1:c.1576+39C>A	XP_011522132.1:n.1576+39C>A
XR_934021.1:n.1781+39C>A
XR_934022.1:n.1687+39C>A
XR_934023.1:n.1687+39C>A
XM_006721516.3:c.1678+39C>A	XP_006721579.2:n.1678+39C>A
XM_011523829.2:c.1576+39C>A	XP_011522131.1:n.1576+39C>A
XM_011523830.2:c.1576+39C>A	XP_011522132.1:n.1576+39C>A
XM_024450741.1:c.1666+39C>A	XP_024306509.1:n.1666+39C>A
XR_934021.2:n.1733+39C>A
XR_934022.2:n.1639+39C>A
XR_934023.2:n.1639+39C>A
NM_000018.4:c.1678+39C>A MANE Select	NP_000009.1:n.1678+39C>A
NM_001033859.3:c.1612+39C>A	NP_001029031.1:n.1612+39C>A
NM_001270447.2:c.1747+39C>A	NP_001257376.1:n.1747+39C>A
NM_001270448.2:c.1450+39C>A	NP_001257377.1:n.1450+39C>A