Canonical Allele Identifier: CA2635784699

Gene: ACADVL

Linked Data

• gnomAD v4: 17-7224584-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7224584C>A , CM000679.2:g.7224584C>A	GRCh38
NC_000017.10:g.7127903C>A , CM000679.1:g.7127903C>A	GRCh37
NC_000017.9:g.7068627C>A	NCBI36
NG_007975.1:g.9751C>A
NG_008391.2:g.467G>T
NG_033038.1:g.14961G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000356839.10:c.1678+32C>A MANE Select	ENSP00000349297.5:n.1678+32C>A
ENST00000322910.9:c.*1633+32C>A	ENSP00000325395.5:n.*1633+32C>A
ENST00000350303.9:c.1612+32C>A	ENSP00000344152.5:n.1612+32C>A
ENST00000356839.9:c.1678+32C>A	ENSP00000349297.5:n.1678+32C>A
ENST00000542255.6:c.536+32C>A
ENST00000543245.6:c.1747+32C>A	ENSP00000438689.2:n.1747+32C>A
ENST00000578319.5:n.259+32C>A
ENST00000578711.1:n.1080C>A
ENST00000578809.5:n.250+32C>A
ENST00000579391.1:n.314C>A
ENST00000579425.5:n.794+32C>A
ENST00000579546.1:c.413+32C>A
ENST00000582450.1:n.218C>A
ENST00000583074.5:n.299+32C>A
ENST00000583848.5:c.64+32C>A	ENSP00000466487.1:n.64+32C>A
ENST00000583850.5:n.449+32C>A
ENST00000583858.5:c.609+32C>A
ENST00000585203.6:n.869+32C>A
NM_000018.3:c.1678+32C>A	NP_000009.1:n.1678+32C>A
NM_001033859.2:c.1612+32C>A	NP_001029031.1:n.1612+32C>A
NM_001270447.1:c.1747+32C>A	NP_001257376.1:n.1747+32C>A
NM_001270448.1:c.1450+32C>A	NP_001257377.1:n.1450+32C>A
XM_006721516.2:c.1678+32C>A	XP_006721579.2:n.1678+32C>A
XM_011523829.1:c.1576+32C>A	XP_011522131.1:n.1576+32C>A
XM_011523830.1:c.1576+32C>A	XP_011522132.1:n.1576+32C>A
XR_934021.1:n.1781+32C>A
XR_934022.1:n.1687+32C>A
XR_934023.1:n.1687+32C>A
XM_006721516.3:c.1678+32C>A	XP_006721579.2:n.1678+32C>A
XM_011523829.2:c.1576+32C>A	XP_011522131.1:n.1576+32C>A
XM_011523830.2:c.1576+32C>A	XP_011522132.1:n.1576+32C>A
XM_024450741.1:c.1666+32C>A	XP_024306509.1:n.1666+32C>A
XR_934021.2:n.1733+32C>A
XR_934022.2:n.1639+32C>A
XR_934023.2:n.1639+32C>A
NM_000018.4:c.1678+32C>A MANE Select	NP_000009.1:n.1678+32C>A
NM_001033859.3:c.1612+32C>A	NP_001029031.1:n.1612+32C>A
NM_001270447.2:c.1747+32C>A	NP_001257376.1:n.1747+32C>A
NM_001270448.2:c.1450+32C>A	NP_001257377.1:n.1450+32C>A