Canonical Allele Identifier: CA2245699485

Gene: ACADVL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7221171_7221173delinsTGG , CM000679.2:g.7221171_7221173delinsTGG	GRCh38
NC_000017.10:g.7124490_7124492delinsTGG , CM000679.1:g.7124490_7124492delinsTGG	GRCh37
NC_000017.9:g.7065214_7065216delinsTGG	NCBI36
NG_007975.1:g.6338_6340delinsTGG
NG_008391.2:g.3878_3880delinsCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.477+113_477+115delinsTGG MANE Select	ENSP00000349297.5:n.477+113_477+115delinsTGG
ENST00000322910.9:c.*432+113_*432+115delinsTGG	ENSP00000325395.5:n.*432+113_*432+115delinsTGG
ENST00000350303.9:c.411+113_411+115delinsTGG	ENSP00000344152.5:n.411+113_411+115delinsTGG
ENST00000356839.9:c.477+113_477+115delinsTGG	ENSP00000349297.5:n.477+113_477+115delinsTGG
ENST00000543245.6:c.546+113_546+115delinsTGG	ENSP00000438689.2:n.546+113_546+115delinsTGG
ENST00000577191.5:n.554+113_554+115delinsTGG
ENST00000577433.5:n.685+113_685+115delinsTGG
ENST00000577857.5:n.293+341_293+343delinsTGG
ENST00000579286.5:n.658+113_658+115delinsTGG
ENST00000579886.2:c.315+113_315+115delinsTGG	ENSP00000463246.1:n.315+113_315+115delinsTGG
ENST00000580365.1:n.208+113_208+115delinsTGG
ENST00000581378.5:c.176+113_176+115delinsTGG
ENST00000581562.5:n.524+113_524+115delinsTGG
ENST00000582166.1:n.458+113_458+115delinsTGG
ENST00000583312.5:c.477+113_477+115delinsTGG	ENSP00000467920.1:n.477+113_477+115delinsTGG
NM_000018.3:c.477+113_477+115delinsTGG	NP_000009.1:n.477+113_477+115delinsTGG
NM_001033859.2:c.411+113_411+115delinsTGG	NP_001029031.1:n.411+113_411+115delinsTGG
NM_001270447.1:c.546+113_546+115delinsTGG	NP_001257376.1:n.546+113_546+115delinsTGG
NM_001270448.1:c.249+113_249+115delinsTGG	NP_001257377.1:n.249+113_249+115delinsTGG
XM_006721516.2:c.477+113_477+115delinsTGG	XP_006721579.2:n.477+113_477+115delinsTGG
XM_011523829.1:c.477+113_477+115delinsTGG	XP_011522131.1:n.477+113_477+115delinsTGG
XM_011523830.1:c.477+113_477+115delinsTGG	XP_011522132.1:n.477+113_477+115delinsTGG
XR_934021.1:n.584+113_584+115delinsTGG
XR_934022.1:n.584+113_584+115delinsTGG
XR_934023.1:n.584+113_584+115delinsTGG
XM_006721516.3:c.477+113_477+115delinsTGG	XP_006721579.2:n.477+113_477+115delinsTGG
XM_011523829.2:c.477+113_477+115delinsTGG	XP_011522131.1:n.477+113_477+115delinsTGG
XM_011523830.2:c.477+113_477+115delinsTGG	XP_011522132.1:n.477+113_477+115delinsTGG
XM_024450741.1:c.477+113_477+115delinsTGG	XP_024306509.1:n.477+113_477+115delinsTGG
XR_934021.2:n.536+113_536+115delinsTGG
XR_934022.2:n.536+113_536+115delinsTGG
XR_934023.2:n.536+113_536+115delinsTGG
NM_000018.4:c.477+113_477+115delinsTGG MANE Select	NP_000009.1:n.477+113_477+115delinsTGG
NM_001033859.3:c.411+113_411+115delinsTGG	NP_001029031.1:n.411+113_411+115delinsTGG
NM_001270447.2:c.546+113_546+115delinsTGG	NP_001257376.1:n.546+113_546+115delinsTGG
NM_001270448.2:c.249+113_249+115delinsTGG	NP_001257377.1:n.249+113_249+115delinsTGG