Canonical Allele Identifier: CA397725570
Gene: ACADVL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224525C>G , CM000679.2:g.7224525C>G GRCh38
NC_000017.10:g.7127844C>G , CM000679.1:g.7127844C>G GRCh37
NC_000017.9:g.7068568C>G NCBI36
NG_007975.1:g.9692C>G
NG_008391.2:g.526G>C
NG_033038.1:g.15020G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1651C>G MANE Select ENSP00000349297.5:p.Leu551Val
ENST00000322910.9:c.*1606C>G ENSP00000325395.5:n.*1606C>G
ENST00000350303.9:c.1585C>G ENSP00000344152.5:p.Leu529Val
ENST00000356839.9:c.1651C>G ENSP00000349297.5:p.Leu551Val
ENST00000542255.6:c.509C>G
ENST00000543245.6:c.1720C>G ENSP00000438689.2:p.Leu574Val
ENST00000578319.5:n.232C>G
ENST00000578711.1:n.1021C>G
ENST00000578809.5:n.223C>G
ENST00000579391.1:n.255C>G
ENST00000579425.5:n.767C>G
ENST00000579546.1:c.386C>G
ENST00000582450.1:n.159C>G
ENST00000583074.5:n.272C>G
ENST00000583848.5:c.37C>G ENSP00000466487.1:p.Leu13Val
ENST00000583850.5:n.422C>G
ENST00000583858.5:c.582C>G
ENST00000585203.6:n.842C>G
NM_000018.3:c.1651C>G NP_000009.1:p.Leu551Val
NM_001033859.2:c.1585C>G NP_001029031.1:p.Leu529Val
NM_001270447.1:c.1720C>G NP_001257376.1:p.Leu574Val
NM_001270448.1:c.1423C>G NP_001257377.1:p.Leu475Val
XM_006721516.2:c.1651C>G XP_006721579.2:p.Leu551Val
XM_011523829.1:c.1549C>G XP_011522131.1:p.Leu517Val
XM_011523830.1:c.1549C>G XP_011522132.1:p.Leu517Val
XR_934021.1:n.1754C>G
XR_934022.1:n.1660C>G
XR_934023.1:n.1660C>G
XM_006721516.3:c.1651C>G XP_006721579.2:p.Leu551Val
XM_011523829.2:c.1549C>G XP_011522131.1:p.Leu517Val
XM_011523830.2:c.1549C>G XP_011522132.1:p.Leu517Val
XM_024450741.1:c.1639C>G XP_024306509.1:p.Leu547Val
XR_934021.2:n.1706C>G
XR_934022.2:n.1612C>G
XR_934023.2:n.1612C>G
NM_000018.4:c.1651C>G MANE Select NP_000009.1:p.Leu551Val
NM_001033859.3:c.1585C>G NP_001029031.1:p.Leu529Val
NM_001270447.2:c.1720C>G NP_001257376.1:p.Leu574Val
NM_001270448.2:c.1423C>G NP_001257377.1:p.Leu475Val