Canonical Allele Identifier: CA2245699886

Gene: ACADVL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7221478_7221481delinsCTGT , CM000679.2:g.7221478_7221481delinsCTGT	GRCh38
NC_000017.10:g.7124797_7124800delinsCTGT , CM000679.1:g.7124797_7124800delinsCTGT	GRCh37
NC_000017.9:g.7065521_7065524delinsCTGT	NCBI36
NG_007975.1:g.6645_6648delinsCTGT
NG_008391.2:g.3570_3573delinsACAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000356839.10:c.478-60_478-57delinsCTGT MANE Select	ENSP00000349297.5:n.478-60_478-57delinsCTGT
ENST00000322910.9:c.*433-60_*433-57delinsCTGT	ENSP00000325395.5:n.*433-60_*433-57delinsCTGT
ENST00000350303.9:c.412-60_412-57delinsCTGT	ENSP00000344152.5:n.412-60_412-57delinsCTGT
ENST00000356839.9:c.478-60_478-57delinsCTGT	ENSP00000349297.5:n.478-60_478-57delinsCTGT
ENST00000543245.6:c.547-60_547-57delinsCTGT	ENSP00000438689.2:n.547-60_547-57delinsCTGT
ENST00000577191.5:n.555-60_555-57delinsCTGT
ENST00000577433.5:n.686-60_686-57delinsCTGT
ENST00000577857.5:n.294-60_294-57delinsCTGT
ENST00000579286.5:n.659-60_659-57delinsCTGT
ENST00000579886.2:c.316-60_316-57delinsCTGT	ENSP00000463246.1:n.316-60_316-57delinsCTGT
ENST00000580365.1:n.209-60_209-57delinsCTGT
ENST00000581378.5:c.177-41_177-38delinsCTGT
ENST00000581562.5:n.524+420_524+423delinsCTGT
ENST00000582166.1:n.459-60_459-57delinsCTGT
ENST00000583312.5:c.478-60_478-57delinsCTGT	ENSP00000467920.1:n.478-60_478-57delinsCTGT
ENST00000583760.1:n.200_203delinsCTGT
NM_000018.3:c.478-60_478-57delinsCTGT	NP_000009.1:n.478-60_478-57delinsCTGT
NM_001033859.2:c.412-60_412-57delinsCTGT	NP_001029031.1:n.412-60_412-57delinsCTGT
NM_001270447.1:c.547-60_547-57delinsCTGT	NP_001257376.1:n.547-60_547-57delinsCTGT
NM_001270448.1:c.250-60_250-57delinsCTGT	NP_001257377.1:n.250-60_250-57delinsCTGT
XM_006721516.2:c.478-60_478-57delinsCTGT	XP_006721579.2:n.478-60_478-57delinsCTGT
XM_011523829.1:c.478-60_478-57delinsCTGT	XP_011522131.1:n.478-60_478-57delinsCTGT
XM_011523830.1:c.478-60_478-57delinsCTGT	XP_011522132.1:n.478-60_478-57delinsCTGT
XR_934021.1:n.585-60_585-57delinsCTGT
XR_934022.1:n.585-60_585-57delinsCTGT
XR_934023.1:n.585-60_585-57delinsCTGT
XM_006721516.3:c.478-60_478-57delinsCTGT	XP_006721579.2:n.478-60_478-57delinsCTGT
XM_011523829.2:c.478-60_478-57delinsCTGT	XP_011522131.1:n.478-60_478-57delinsCTGT
XM_011523830.2:c.478-60_478-57delinsCTGT	XP_011522132.1:n.478-60_478-57delinsCTGT
XM_024450741.1:c.478-60_478-57delinsCTGT	XP_024306509.1:n.478-60_478-57delinsCTGT
XR_934021.2:n.537-60_537-57delinsCTGT
XR_934022.2:n.537-60_537-57delinsCTGT
XR_934023.2:n.537-60_537-57delinsCTGT
NM_000018.4:c.478-60_478-57delinsCTGT MANE Select	NP_000009.1:n.478-60_478-57delinsCTGT
NM_001033859.3:c.412-60_412-57delinsCTGT	NP_001029031.1:n.412-60_412-57delinsCTGT
NM_001270447.2:c.547-60_547-57delinsCTGT	NP_001257376.1:n.547-60_547-57delinsCTGT
NM_001270448.2:c.250-60_250-57delinsCTGT	NP_001257377.1:n.250-60_250-57delinsCTGT