Canonical Allele Identifier: CA397722618
Gene: ACADVL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7220827C>G , CM000679.2:g.7220827C>G GRCh38
NC_000017.10:g.7124146C>G , CM000679.1:g.7124146C>G GRCh37
NC_000017.9:g.7064870C>G NCBI36
NG_007975.1:g.5994C>G
NG_008391.2:g.4224G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.339C>G MANE Select ENSP00000349297.5:p.Phe113Leu
ENST00000322910.9:c.*294C>G ENSP00000325395.5:n.*294C>G
ENST00000350303.9:c.273C>G ENSP00000344152.5:p.Phe91Leu
ENST00000356839.9:c.339C>G ENSP00000349297.5:p.Phe113Leu
ENST00000543245.6:c.408C>G ENSP00000438689.2:p.Phe136Leu
ENST00000577191.5:n.416C>G
ENST00000577433.5:n.547C>G
ENST00000577857.5:n.290C>G
ENST00000579286.5:n.520C>G
ENST00000579886.2:c.202-118C>G ENSP00000463246.1:n.202-118C>G
ENST00000580365.1:n.70C>G
ENST00000581378.5:c.38C>G
ENST00000581562.5:n.386C>G
ENST00000582056.5:n.429C>G
ENST00000582166.1:n.227C>G
ENST00000582356.5:n.538C>G
ENST00000583312.5:c.339C>G ENSP00000467920.1:p.Phe113Leu
ENST00000584103.5:c.339C>G ENSP00000465353.1:p.Phe113Leu
NM_000018.3:c.339C>G NP_000009.1:p.Phe113Leu
NM_001033859.2:c.273C>G NP_001029031.1:p.Phe91Leu
NM_001270447.1:c.408C>G NP_001257376.1:p.Phe136Leu
NM_001270448.1:c.111C>G NP_001257377.1:p.Phe37Leu
XM_006721516.2:c.339C>G XP_006721579.2:p.Phe113Leu
XM_011523829.1:c.339C>G XP_011522131.1:p.Phe113Leu
XM_011523830.1:c.339C>G XP_011522132.1:p.Phe113Leu
XR_934021.1:n.446C>G
XR_934022.1:n.446C>G
XR_934023.1:n.446C>G
XM_006721516.3:c.339C>G XP_006721579.2:p.Phe113Leu
XM_011523829.2:c.339C>G XP_011522131.1:p.Phe113Leu
XM_011523830.2:c.339C>G XP_011522132.1:p.Phe113Leu
XM_024450741.1:c.339C>G XP_024306509.1:p.Phe113Leu
XR_934021.2:n.398C>G
XR_934022.2:n.398C>G
XR_934023.2:n.398C>G
NM_000018.4:c.339C>G MANE Select NP_000009.1:p.Phe113Leu
NM_001033859.3:c.273C>G NP_001029031.1:p.Phe91Leu
NM_001270447.2:c.408C>G NP_001257376.1:p.Phe136Leu
NM_001270448.2:c.111C>G NP_001257377.1:p.Phe37Leu