Canonical Allele Identifier: CA497694302
Gene: ACADVL HGNC NCBI

Linked Data

dbSNP Id: rs1232379348
gnomAD v2: 17-7127530-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224211C>T , CM000679.2:g.7224211C>T GRCh38
NC_000017.10:g.7127530C>T , CM000679.1:g.7127530C>T GRCh37
NC_000017.9:g.7068254C>T NCBI36
NG_007975.1:g.9378C>T
NG_008391.2:g.840G>A
NG_033038.1:g.15334G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1500C>T MANE Select ENSP00000349297.5:p.Leu500=
ENST00000322910.9:c.*1455C>T ENSP00000325395.5:n.*1455C>T
ENST00000350303.9:c.1434C>T ENSP00000344152.5:p.Leu478=
ENST00000356839.9:c.1500C>T ENSP00000349297.5:p.Leu500=
ENST00000542255.6:c.358C>T
ENST00000543245.6:c.1569C>T ENSP00000438689.2:p.Leu523=
ENST00000578711.1:n.707C>T
ENST00000579391.1:n.108C>T
ENST00000579425.5:n.616C>T
ENST00000579546.1:c.272-110C>T
ENST00000579894.5:n.287C>T
ENST00000583074.5:n.154-110C>T
ENST00000583850.5:n.275C>T
ENST00000583858.5:c.464-110C>T
ENST00000585203.6:n.691C>T
NM_000018.3:c.1500C>T NP_000009.1:p.Leu500=
NM_001033859.2:c.1434C>T NP_001029031.1:p.Leu478=
NM_001270447.1:c.1569C>T NP_001257376.1:p.Leu523=
NM_001270448.1:c.1272C>T NP_001257377.1:p.Leu424=
XM_006721516.2:c.1500C>T XP_006721579.2:p.Leu500=
XM_011523829.1:c.1435-110C>T XP_011522131.1:n.1435-110C>T
XM_011523830.1:c.1435-110C>T XP_011522132.1:n.1435-110C>T
XR_934021.1:n.1607C>T
XR_934022.1:n.1542-110C>T
XR_934023.1:n.1542-110C>T
XM_006721516.3:c.1500C>T XP_006721579.2:p.Leu500=
XM_011523829.2:c.1435-110C>T XP_011522131.1:n.1435-110C>T
XM_011523830.2:c.1435-110C>T XP_011522132.1:n.1435-110C>T
XM_024450741.1:c.1435-110C>T XP_024306509.1:n.1435-110C>T
XR_934021.2:n.1559C>T
XR_934022.2:n.1494-110C>T
XR_934023.2:n.1494-110C>T
NM_000018.4:c.1500C>T MANE Select NP_000009.1:p.Leu500=
NM_001033859.3:c.1434C>T NP_001029031.1:p.Leu478=
NM_001270447.2:c.1569C>T NP_001257376.1:p.Leu523=
NM_001270448.2:c.1272C>T NP_001257377.1:p.Leu424=