Canonical Allele Identifier: CA397725641
Gene: ACADVL HGNC NCBI

Linked Data

gnomAD v4: 17-7224641-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224641G>T , CM000679.2:g.7224641G>T GRCh38
NC_000017.10:g.7127960G>T , CM000679.1:g.7127960G>T GRCh37
NC_000017.9:g.7068684G>T NCBI36
NG_007975.1:g.9808G>T
NG_008391.2:g.410C>A
NG_033038.1:g.14904C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000356839.10:c.1679-1G>T MANE Select ENSP00000349297.5:n.1679-1G>T
ENST00000322910.9:c.*1634-1G>T ENSP00000325395.5:n.*1634-1G>T
ENST00000350303.9:c.1613-1G>T ENSP00000344152.5:n.1613-1G>T
ENST00000356839.9:c.1679-1G>T ENSP00000349297.5:n.1679-1G>T
ENST00000542255.6:c.537-74G>T
ENST00000543245.6:c.1748-1G>T ENSP00000438689.2:n.1748-1G>T
ENST00000578033.1:n.9G>T
ENST00000578319.5:n.260-1G>T
ENST00000578711.1:n.1137G>T
ENST00000578809.5:n.251-1G>T
ENST00000579425.5:n.795-1G>T
ENST00000579546.1:c.414-1G>T
ENST00000582450.1:n.275G>T
ENST00000583074.5:n.300-74G>T
ENST00000583848.5:c.65-21G>T ENSP00000466487.1:n.65-21G>T
ENST00000583850.5:n.450-1G>T
ENST00000583858.5:c.610-1G>T
ENST00000585203.6:n.870-1G>T
NM_000018.3:c.1679-1G>T NP_000009.1:n.1679-1G>T
NM_001033859.2:c.1613-1G>T NP_001029031.1:n.1613-1G>T
NM_001270447.1:c.1748-1G>T NP_001257376.1:n.1748-1G>T
NM_001270448.1:c.1451-1G>T NP_001257377.1:n.1451-1G>T
XM_006721516.2:c.1679-74G>T XP_006721579.2:n.1679-74G>T
XM_011523829.1:c.1577-74G>T XP_011522131.1:n.1577-74G>T
XM_011523830.1:c.1577-1G>T XP_011522132.1:n.1577-1G>T
XR_934021.1:n.1782-1G>T
XR_934022.1:n.1688-1G>T
XR_934023.1:n.1688-74G>T
XM_006721516.3:c.1679-74G>T XP_006721579.2:n.1679-74G>T
XM_011523829.2:c.1577-74G>T XP_011522131.1:n.1577-74G>T
XM_011523830.2:c.1577-1G>T XP_011522132.1:n.1577-1G>T
XM_024450741.1:c.1667-1G>T XP_024306509.1:n.1667-1G>T
XR_934021.2:n.1734-1G>T
XR_934022.2:n.1640-1G>T
XR_934023.2:n.1640-74G>T
NM_000018.4:c.1679-1G>T MANE Select NP_000009.1:n.1679-1G>T
NM_001033859.3:c.1613-1G>T NP_001029031.1:n.1613-1G>T
NM_001270447.2:c.1748-1G>T NP_001257376.1:n.1748-1G>T
NM_001270448.2:c.1451-1G>T NP_001257377.1:n.1451-1G>T