Canonical Allele Identifier: CA2245699775

Gene: ACADVL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7221425_7221440delinsCCCTAGGTCAGGAACT , CM000679.2:g.7221425_7221440delinsCCCTAGGTCAGGAACT	GRCh38
NC_000017.10:g.7124744_7124759delinsCCCTAGGTCAGGAACT , CM000679.1:g.7124744_7124759delinsCCCTAGGTCAGGAACT	GRCh37
NC_000017.9:g.7065468_7065483delinsCCCTAGGTCAGGAACT	NCBI36
NG_007975.1:g.6592_6607delinsCCCTAGGTCAGGAACT
NG_008391.2:g.3611_3626delinsAGTTCCTGACCTAGGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000356839.10:c.478-113_478-98delinsCCCTAGGTCAGGAACT MANE Select	ENSP00000349297.5:n.478-113_478-98delinsC...
ENST00000322910.9:c.*433-113_*433-98delinsCCCTAGGTCAGGAACT	ENSP00000325395.5:n.*433-113_*433-98delin...
ENST00000350303.9:c.412-113_412-98delinsCCCTAGGTCAGGAACT	ENSP00000344152.5:n.412-113_412-98delinsC...
ENST00000356839.9:c.478-113_478-98delinsCCCTAGGTCAGGAACT	ENSP00000349297.5:n.478-113_478-98delinsC...
ENST00000543245.6:c.547-113_547-98delinsCCCTAGGTCAGGAACT	ENSP00000438689.2:n.547-113_547-98delinsC...
ENST00000577191.5:n.555-113_555-98delinsCCCTAGGTCAGGAACT
ENST00000577433.5:n.686-113_686-98delinsCCCTAGGTCAGGAACT
ENST00000577857.5:n.294-113_294-98delinsCCCTAGGTCAGGAACT
ENST00000579286.5:n.659-113_659-98delinsCCCTAGGTCAGGAACT
ENST00000579886.2:c.316-113_316-98delinsCCCTAGGTCAGGAACT	ENSP00000463246.1:n.316-113_316-98delinsC...
ENST00000580365.1:n.209-113_209-98delinsCCCTAGGTCAGGAACT
ENST00000581378.5:c.177-94_177-79delinsCCCTAGGTCAGGAACT
ENST00000581562.5:n.524+367_524+382delinsCCCTAGGTCAGGAACT
ENST00000582166.1:n.459-113_459-98delinsCCCTAGGTCAGGAACT
ENST00000583312.5:c.478-113_478-98delinsCCCTAGGTCAGGAACT	ENSP00000467920.1:n.478-113_478-98delinsC...
ENST00000583760.1:n.147_162delinsCCCTAGGTCAGGAACT
NM_000018.3:c.478-113_478-98delinsCCCTAGGTCAGGAACT	NP_000009.1:n.478-113_478-98delinsCCCTAGG...
NM_001033859.2:c.412-113_412-98delinsCCCTAGGTCAGGAACT	NP_001029031.1:n.412-113_412-98delinsCCCT...
NM_001270447.1:c.547-113_547-98delinsCCCTAGGTCAGGAACT	NP_001257376.1:n.547-113_547-98delinsCCCT...
NM_001270448.1:c.250-113_250-98delinsCCCTAGGTCAGGAACT	NP_001257377.1:n.250-113_250-98delinsCCCT...
XM_006721516.2:c.478-113_478-98delinsCCCTAGGTCAGGAACT	XP_006721579.2:n.478-113_478-98delinsCCCT...
XM_011523829.1:c.478-113_478-98delinsCCCTAGGTCAGGAACT	XP_011522131.1:n.478-113_478-98delinsCCCT...
XM_011523830.1:c.478-113_478-98delinsCCCTAGGTCAGGAACT	XP_011522132.1:n.478-113_478-98delinsCCCT...
XR_934021.1:n.585-113_585-98delinsCCCTAGGTCAGGAACT
XR_934022.1:n.585-113_585-98delinsCCCTAGGTCAGGAACT
XR_934023.1:n.585-113_585-98delinsCCCTAGGTCAGGAACT
XM_006721516.3:c.478-113_478-98delinsCCCTAGGTCAGGAACT	XP_006721579.2:n.478-113_478-98delinsCCCT...
XM_011523829.2:c.478-113_478-98delinsCCCTAGGTCAGGAACT	XP_011522131.1:n.478-113_478-98delinsCCCT...
XM_011523830.2:c.478-113_478-98delinsCCCTAGGTCAGGAACT	XP_011522132.1:n.478-113_478-98delinsCCCT...
XM_024450741.1:c.478-113_478-98delinsCCCTAGGTCAGGAACT	XP_024306509.1:n.478-113_478-98delinsCCCT...
XR_934021.2:n.537-113_537-98delinsCCCTAGGTCAGGAACT
XR_934022.2:n.537-113_537-98delinsCCCTAGGTCAGGAACT
XR_934023.2:n.537-113_537-98delinsCCCTAGGTCAGGAACT
NM_000018.4:c.478-113_478-98delinsCCCTAGGTCAGGAACT MANE Select	NP_000009.1:n.478-113_478-98delinsCCCTAGG...
NM_001033859.3:c.412-113_412-98delinsCCCTAGGTCAGGAACT	NP_001029031.1:n.412-113_412-98delinsCCCT...
NM_001270447.2:c.547-113_547-98delinsCCCTAGGTCAGGAACT	NP_001257376.1:n.547-113_547-98delinsCCCT...
NM_001270448.2:c.250-113_250-98delinsCCCTAGGTCAGGAACT	NP_001257377.1:n.250-113_250-98delinsCCCT...