Canonical Allele Identifier: CA2635780717
Gene: ACADVL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221230dup , CM000679.2:g.7221230dup GRCh38
NC_000017.10:g.7124549dup , CM000679.1:g.7124549dup GRCh37
NC_000017.9:g.7065273dup NCBI36
NG_007975.1:g.6397dup
NG_008391.2:g.3824dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.477+172dup MANE Select ENSP00000349297.5:n.477+172dup
ENST00000322910.9:c.*432+172dup ENSP00000325395.5:n.*432+172dup
ENST00000350303.9:c.411+172dup ENSP00000344152.5:n.411+172dup
ENST00000356839.9:c.477+172dup ENSP00000349297.5:n.477+172dup
ENST00000543245.6:c.546+172dup ENSP00000438689.2:n.546+172dup
ENST00000577191.5:n.554+172dup
ENST00000577433.5:n.685+172dup
ENST00000577857.5:n.294-308dup
ENST00000579286.5:n.658+172dup
ENST00000579886.2:c.315+172dup ENSP00000463246.1:n.315+172dup
ENST00000580365.1:n.208+172dup
ENST00000581378.5:c.176+172dup
ENST00000581562.5:n.524+172dup
ENST00000582166.1:n.458+172dup
ENST00000583312.5:c.477+172dup ENSP00000467920.1:n.477+172dup
NM_000018.3:c.477+172dup NP_000009.1:n.477+172dup
NM_001033859.2:c.411+172dup NP_001029031.1:n.411+172dup
NM_001270447.1:c.546+172dup NP_001257376.1:n.546+172dup
NM_001270448.1:c.249+172dup NP_001257377.1:n.249+172dup
XM_006721516.2:c.477+172dup XP_006721579.2:n.477+172dup
XM_011523829.1:c.477+172dup XP_011522131.1:n.477+172dup
XM_011523830.1:c.477+172dup XP_011522132.1:n.477+172dup
XR_934021.1:n.584+172dup
XR_934022.1:n.584+172dup
XR_934023.1:n.584+172dup
XM_006721516.3:c.477+172dup XP_006721579.2:n.477+172dup
XM_011523829.2:c.477+172dup XP_011522131.1:n.477+172dup
XM_011523830.2:c.477+172dup XP_011522132.1:n.477+172dup
XM_024450741.1:c.477+172dup XP_024306509.1:n.477+172dup
XR_934021.2:n.536+172dup
XR_934022.2:n.536+172dup
XR_934023.2:n.536+172dup
NM_000018.4:c.477+172dup MANE Select NP_000009.1:n.477+172dup
NM_001033859.3:c.411+172dup NP_001029031.1:n.411+172dup
NM_001270447.2:c.546+172dup NP_001257376.1:n.546+172dup
NM_001270448.2:c.249+172dup NP_001257377.1:n.249+172dup