Canonical Allele Identifier: CA2635784700

Gene: ACADVL

Linked Data

• gnomAD v4: 17-7224584-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7224587del , CM000679.2:g.7224587del	GRCh38
NC_000017.10:g.7127906del , CM000679.1:g.7127906del	GRCh37
NC_000017.9:g.7068630del	NCBI36
NG_007975.1:g.9754del
NG_008391.2:g.466del
NG_033038.1:g.14960del

Transcript Alleles

HGVS	Amino-acid change
ENST00000356839.10:c.1678+35del MANE Select	ENSP00000349297.5:n.1678+35del
ENST00000322910.9:c.*1633+35del	ENSP00000325395.5:n.*1633+35del
ENST00000350303.9:c.1612+35del	ENSP00000344152.5:n.1612+35del
ENST00000356839.9:c.1678+35del	ENSP00000349297.5:n.1678+35del
ENST00000542255.6:c.536+35del
ENST00000543245.6:c.1747+35del	ENSP00000438689.2:n.1747+35del
ENST00000578319.5:n.259+35del
ENST00000578711.1:n.1083del
ENST00000578809.5:n.250+35del
ENST00000579391.1:n.317del
ENST00000579425.5:n.794+35del
ENST00000579546.1:c.413+35del
ENST00000582450.1:n.221del
ENST00000583074.5:n.299+35del
ENST00000583848.5:c.64+35del	ENSP00000466487.1:n.64+35del
ENST00000583850.5:n.449+35del
ENST00000583858.5:c.609+35del
ENST00000585203.6:n.869+35del
NM_000018.3:c.1678+35del	NP_000009.1:n.1678+35del
NM_001033859.2:c.1612+35del	NP_001029031.1:n.1612+35del
NM_001270447.1:c.1747+35del	NP_001257376.1:n.1747+35del
NM_001270448.1:c.1450+35del	NP_001257377.1:n.1450+35del
XM_006721516.2:c.1678+35del	XP_006721579.2:n.1678+35del
XM_011523829.1:c.1576+35del	XP_011522131.1:n.1576+35del
XM_011523830.1:c.1576+35del	XP_011522132.1:n.1576+35del
XR_934021.1:n.1781+35del
XR_934022.1:n.1687+35del
XR_934023.1:n.1687+35del
XM_006721516.3:c.1678+35del	XP_006721579.2:n.1678+35del
XM_011523829.2:c.1576+35del	XP_011522131.1:n.1576+35del
XM_011523830.2:c.1576+35del	XP_011522132.1:n.1576+35del
XM_024450741.1:c.1666+35del	XP_024306509.1:n.1666+35del
XR_934021.2:n.1733+35del
XR_934022.2:n.1639+35del
XR_934023.2:n.1639+35del
NM_000018.4:c.1678+35del MANE Select	NP_000009.1:n.1678+35del
NM_001033859.3:c.1612+35del	NP_001029031.1:n.1612+35del
NM_001270447.2:c.1747+35del	NP_001257376.1:n.1747+35del
NM_001270448.2:c.1450+35del	NP_001257377.1:n.1450+35del