Canonical Allele Identifier: CA2635784761

Gene: ACADVL

Linked Data

• gnomAD v4: 17-7224597-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7224597G>T , CM000679.2:g.7224597G>T	GRCh38
NC_000017.10:g.7127916G>T , CM000679.1:g.7127916G>T	GRCh37
NC_000017.9:g.7068640G>T	NCBI36
NG_007975.1:g.9764G>T
NG_008391.2:g.454C>A
NG_033038.1:g.14948C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000356839.10:c.1679-45G>T MANE Select	ENSP00000349297.5:n.1679-45G>T
ENST00000322910.9:c.*1634-45G>T	ENSP00000325395.5:n.*1634-45G>T
ENST00000350303.9:c.1613-45G>T	ENSP00000344152.5:n.1613-45G>T
ENST00000356839.9:c.1679-45G>T	ENSP00000349297.5:n.1679-45G>T
ENST00000542255.6:c.536+45G>T
ENST00000543245.6:c.1748-45G>T	ENSP00000438689.2:n.1748-45G>T
ENST00000578319.5:n.260-45G>T
ENST00000578711.1:n.1093G>T
ENST00000578809.5:n.251-45G>T
ENST00000579391.1:n.327G>T
ENST00000579425.5:n.795-45G>T
ENST00000579546.1:c.414-45G>T
ENST00000582450.1:n.231G>T
ENST00000583074.5:n.299+45G>T
ENST00000583848.5:c.64+45G>T	ENSP00000466487.1:n.64+45G>T
ENST00000583850.5:n.450-45G>T
ENST00000583858.5:c.610-45G>T
ENST00000585203.6:n.870-45G>T
NM_000018.3:c.1679-45G>T	NP_000009.1:n.1679-45G>T
NM_001033859.2:c.1613-45G>T	NP_001029031.1:n.1613-45G>T
NM_001270447.1:c.1748-45G>T	NP_001257376.1:n.1748-45G>T
NM_001270448.1:c.1451-45G>T	NP_001257377.1:n.1451-45G>T
XM_006721516.2:c.1678+45G>T	XP_006721579.2:n.1678+45G>T
XM_011523829.1:c.1576+45G>T	XP_011522131.1:n.1576+45G>T
XM_011523830.1:c.1577-45G>T	XP_011522132.1:n.1577-45G>T
XR_934021.1:n.1782-45G>T
XR_934022.1:n.1688-45G>T
XR_934023.1:n.1687+45G>T
XM_006721516.3:c.1678+45G>T	XP_006721579.2:n.1678+45G>T
XM_011523829.2:c.1576+45G>T	XP_011522131.1:n.1576+45G>T
XM_011523830.2:c.1577-45G>T	XP_011522132.1:n.1577-45G>T
XM_024450741.1:c.1667-45G>T	XP_024306509.1:n.1667-45G>T
XR_934021.2:n.1734-45G>T
XR_934022.2:n.1640-45G>T
XR_934023.2:n.1639+45G>T
NM_000018.4:c.1679-45G>T MANE Select	NP_000009.1:n.1679-45G>T
NM_001033859.3:c.1613-45G>T	NP_001029031.1:n.1613-45G>T
NM_001270447.2:c.1748-45G>T	NP_001257376.1:n.1748-45G>T
NM_001270448.2:c.1451-45G>T	NP_001257377.1:n.1451-45G>T