Canonical Allele Identifier: CA2808365793

Gene: ACADVL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7221206_7221207insCACC , CM000679.2:g.7221206_7221207insCACC	GRCh38
NC_000017.10:g.7124525_7124526insCACC , CM000679.1:g.7124525_7124526insCACC	GRCh37
NC_000017.9:g.7065249_7065250insCACC	NCBI36
NG_007975.1:g.6373_6374insCACC
NG_008391.2:g.3844_3845insGGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.477+148_477+149insCACC MANE Select	ENSP00000349297.5:n.477+148_477+149insCACC
ENST00000322910.9:c.*432+148_*432+149insCACC	ENSP00000325395.5:n.*432+148_*432+149insCACC
ENST00000350303.9:c.411+148_411+149insCACC	ENSP00000344152.5:n.411+148_411+149insCACC
ENST00000356839.9:c.477+148_477+149insCACC	ENSP00000349297.5:n.477+148_477+149insCACC
ENST00000543245.6:c.546+148_546+149insCACC	ENSP00000438689.2:n.546+148_546+149insCACC
ENST00000577191.5:n.554+148_554+149insCACC
ENST00000577433.5:n.685+148_685+149insCACC
ENST00000577857.5:n.294-332_294-331insCACC
ENST00000579286.5:n.658+148_658+149insCACC
ENST00000579886.2:c.315+148_315+149insCACC	ENSP00000463246.1:n.315+148_315+149insCACC
ENST00000580365.1:n.208+148_208+149insCACC
ENST00000581378.5:c.176+148_176+149insCACC
ENST00000581562.5:n.524+148_524+149insCACC
ENST00000582166.1:n.458+148_458+149insCACC
ENST00000583312.5:c.477+148_477+149insCACC	ENSP00000467920.1:n.477+148_477+149insCACC
NM_000018.3:c.477+148_477+149insCACC	NP_000009.1:n.477+148_477+149insCACC
NM_001033859.2:c.411+148_411+149insCACC	NP_001029031.1:n.411+148_411+149insCACC
NM_001270447.1:c.546+148_546+149insCACC	NP_001257376.1:n.546+148_546+149insCACC
NM_001270448.1:c.249+148_249+149insCACC	NP_001257377.1:n.249+148_249+149insCACC
XM_006721516.2:c.477+148_477+149insCACC	XP_006721579.2:n.477+148_477+149insCACC
XM_011523829.1:c.477+148_477+149insCACC	XP_011522131.1:n.477+148_477+149insCACC
XM_011523830.1:c.477+148_477+149insCACC	XP_011522132.1:n.477+148_477+149insCACC
XR_934021.1:n.584+148_584+149insCACC
XR_934022.1:n.584+148_584+149insCACC
XR_934023.1:n.584+148_584+149insCACC
XM_006721516.3:c.477+148_477+149insCACC	XP_006721579.2:n.477+148_477+149insCACC
XM_011523829.2:c.477+148_477+149insCACC	XP_011522131.1:n.477+148_477+149insCACC
XM_011523830.2:c.477+148_477+149insCACC	XP_011522132.1:n.477+148_477+149insCACC
XM_024450741.1:c.477+148_477+149insCACC	XP_024306509.1:n.477+148_477+149insCACC
XR_934021.2:n.536+148_536+149insCACC
XR_934022.2:n.536+148_536+149insCACC
XR_934023.2:n.536+148_536+149insCACC
NM_000018.4:c.477+148_477+149insCACC MANE Select	NP_000009.1:n.477+148_477+149insCACC
NM_001033859.3:c.411+148_411+149insCACC	NP_001029031.1:n.411+148_411+149insCACC
NM_001270447.2:c.546+148_546+149insCACC	NP_001257376.1:n.546+148_546+149insCACC
NM_001270448.2:c.249+148_249+149insCACC	NP_001257377.1:n.249+148_249+149insCACC