Canonical Allele Identifier: CA397723603
Gene: ACADVL HGNC NCBI

Linked Data

gnomAD v4: 17-7222081-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222081G>A , CM000679.2:g.7222081G>A GRCh38
NC_000017.10:g.7125400G>A , CM000679.1:g.7125400G>A GRCh37
NC_000017.9:g.7066124G>A NCBI36
NG_007975.1:g.7248G>A
NG_008391.2:g.2970C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000356839.10:c.752G>A MANE Select ENSP00000349297.5:p.Ser251Asn
ENST00000322910.9:c.*707G>A ENSP00000325395.5:n.*707G>A
ENST00000350303.9:c.686G>A ENSP00000344152.5:p.Ser229Asn
ENST00000356839.9:c.752G>A ENSP00000349297.5:p.Ser251Asn
ENST00000543245.6:c.821G>A ENSP00000438689.2:p.Ser274Asn
ENST00000577191.5:n.829G>A
ENST00000579286.5:n.933G>A
ENST00000580365.1:n.483G>A
ENST00000581378.5:c.470G>A
ENST00000582379.1:n.136G>A
ENST00000583760.1:n.534G>A
NM_000018.3:c.752G>A NP_000009.1:p.Ser251Asn
NM_001033859.2:c.686G>A NP_001029031.1:p.Ser229Asn
NM_001270447.1:c.821G>A NP_001257376.1:p.Ser274Asn
NM_001270448.1:c.524G>A NP_001257377.1:p.Ser175Asn
XM_006721516.2:c.752G>A XP_006721579.2:p.Ser251Asn
XM_011523829.1:c.752G>A XP_011522131.1:p.Ser251Asn
XM_011523830.1:c.752G>A XP_011522132.1:p.Ser251Asn
XR_934021.1:n.859G>A
XR_934022.1:n.859G>A
XR_934023.1:n.859G>A
XM_006721516.3:c.752G>A XP_006721579.2:p.Ser251Asn
XM_011523829.2:c.752G>A XP_011522131.1:p.Ser251Asn
XM_011523830.2:c.752G>A XP_011522132.1:p.Ser251Asn
XM_024450741.1:c.752G>A XP_024306509.1:p.Ser251Asn
XR_934021.2:n.811G>A
XR_934022.2:n.811G>A
XR_934023.2:n.811G>A
NM_000018.4:c.752G>A MANE Select NP_000009.1:p.Ser251Asn
NM_001033859.3:c.686G>A NP_001029031.1:p.Ser229Asn
NM_001270447.2:c.821G>A NP_001257376.1:p.Ser274Asn
NM_001270448.2:c.524G>A NP_001257377.1:p.Ser175Asn