Canonical Allele Identifier: CA2245699591
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221273C= , CM000679.2:g.7221273C= GRCh38
NC_000017.10:g.7124592C= , CM000679.1:g.7124592C= GRCh37
NC_000017.9:g.7065316C= NCBI36
NG_007975.1:g.6440C=
NG_008391.2:g.3778G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.477+215C= MANE Select ENSP00000349297.5:n.477+215C=
ENST00000322910.9:c.*432+215C= ENSP00000325395.5:n.*432+215C=
ENST00000350303.9:c.411+215C= ENSP00000344152.5:n.411+215C=
ENST00000356839.9:c.477+215C= ENSP00000349297.5:n.477+215C=
ENST00000543245.6:c.546+215C= ENSP00000438689.2:n.546+215C=
ENST00000577191.5:n.554+215C=
ENST00000577433.5:n.685+215C=
ENST00000577857.5:n.294-265C=
ENST00000579286.5:n.658+215C=
ENST00000579886.2:c.315+215C= ENSP00000463246.1:n.315+215C=
ENST00000580365.1:n.208+215C=
ENST00000581378.5:c.176+215C=
ENST00000581562.5:n.524+215C=
ENST00000582166.1:n.458+215C=
ENST00000583312.5:c.477+215C= ENSP00000467920.1:n.477+215C=
NM_000018.3:c.477+215C= NP_000009.1:n.477+215C=
NM_001033859.2:c.411+215C= NP_001029031.1:n.411+215C=
NM_001270447.1:c.546+215C= NP_001257376.1:n.546+215C=
NM_001270448.1:c.249+215C= NP_001257377.1:n.249+215C=
XM_006721516.2:c.477+215C= XP_006721579.2:n.477+215C=
XM_011523829.1:c.477+215C= XP_011522131.1:n.477+215C=
XM_011523830.1:c.477+215C= XP_011522132.1:n.477+215C=
XR_934021.1:n.584+215C=
XR_934022.1:n.584+215C=
XR_934023.1:n.584+215C=
XM_006721516.3:c.477+215C= XP_006721579.2:n.477+215C=
XM_011523829.2:c.477+215C= XP_011522131.1:n.477+215C=
XM_011523830.2:c.477+215C= XP_011522132.1:n.477+215C=
XM_024450741.1:c.477+215C= XP_024306509.1:n.477+215C=
XR_934021.2:n.536+215C=
XR_934022.2:n.536+215C=
XR_934023.2:n.536+215C=
NM_000018.4:c.477+215C= MANE Select NP_000009.1:n.477+215C=
NM_001033859.3:c.411+215C= NP_001029031.1:n.411+215C=
NM_001270447.2:c.546+215C= NP_001257376.1:n.546+215C=
NM_001270448.2:c.249+215C= NP_001257377.1:n.249+215C=