Canonical Allele Identifier: CA397723170
Gene: ACADVL HGNC NCBI

Linked Data

ClinVar Variation Id: 838654
ClinVar RCV Id: RCV001040243
dbSNP Id: rs2071231356

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221622G>A , CM000679.2:g.7221622G>A GRCh38
NC_000017.10:g.7124941G>A , CM000679.1:g.7124941G>A GRCh37
NC_000017.9:g.7065665G>A NCBI36
NG_007975.1:g.6789G>A
NG_008391.2:g.3429C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000356839.10:c.562G>A MANE Select ENSP00000349297.5:p.Gly188Ser
ENST00000322910.9:c.*517G>A ENSP00000325395.5:n.*517G>A
ENST00000350303.9:c.496G>A ENSP00000344152.5:p.Gly166Ser
ENST00000356839.9:c.562G>A ENSP00000349297.5:p.Gly188Ser
ENST00000543245.6:c.631G>A ENSP00000438689.2:p.Gly211Ser
ENST00000577191.5:n.639G>A
ENST00000577433.5:n.770G>A
ENST00000577857.5:n.378G>A
ENST00000579286.5:n.743G>A
ENST00000579886.2:c.400G>A ENSP00000463246.1:p.Gly134Ser
ENST00000580365.1:n.293G>A
ENST00000581378.5:c.280G>A
ENST00000581562.5:n.525-330G>A
ENST00000582166.1:n.543G>A
ENST00000583312.5:c.562G>A ENSP00000467920.1:p.Gly188Ser
ENST00000583760.1:n.344G>A
NM_000018.3:c.562G>A NP_000009.1:p.Gly188Ser
NM_001033859.2:c.496G>A NP_001029031.1:p.Gly166Ser
NM_001270447.1:c.631G>A NP_001257376.1:p.Gly211Ser
NM_001270448.1:c.334G>A NP_001257377.1:p.Gly112Ser
XM_006721516.2:c.562G>A XP_006721579.2:p.Gly188Ser
XM_011523829.1:c.562G>A XP_011522131.1:p.Gly188Ser
XM_011523830.1:c.562G>A XP_011522132.1:p.Gly188Ser
XR_934021.1:n.669G>A
XR_934022.1:n.669G>A
XR_934023.1:n.669G>A
XM_006721516.3:c.562G>A XP_006721579.2:p.Gly188Ser
XM_011523829.2:c.562G>A XP_011522131.1:p.Gly188Ser
XM_011523830.2:c.562G>A XP_011522132.1:p.Gly188Ser
XM_024450741.1:c.562G>A XP_024306509.1:p.Gly188Ser
XR_934021.2:n.621G>A
XR_934022.2:n.621G>A
XR_934023.2:n.621G>A
NM_000018.4:c.562G>A MANE Select NP_000009.1:p.Gly188Ser
NM_001033859.3:c.496G>A NP_001029031.1:p.Gly166Ser
NM_001270447.2:c.631G>A NP_001257376.1:p.Gly211Ser
NM_001270448.2:c.334G>A NP_001257377.1:p.Gly112Ser