Canonical Allele Identifier: CA2245699856

Gene: ACADVL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7221468_7221470delinsCCA , CM000679.2:g.7221468_7221470delinsCCA	GRCh38
NC_000017.10:g.7124787_7124789delinsCCA , CM000679.1:g.7124787_7124789delinsCCA	GRCh37
NC_000017.9:g.7065511_7065513delinsCCA	NCBI36
NG_007975.1:g.6635_6637delinsCCA
NG_008391.2:g.3581_3583delinsTGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000356839.10:c.478-70_478-68delinsCCA MANE Select	ENSP00000349297.5:n.478-70_478-68delinsCCA
ENST00000322910.9:c.*433-70_*433-68delinsCCA	ENSP00000325395.5:n.*433-70_*433-68delinsCCA
ENST00000350303.9:c.412-70_412-68delinsCCA	ENSP00000344152.5:n.412-70_412-68delinsCCA
ENST00000356839.9:c.478-70_478-68delinsCCA	ENSP00000349297.5:n.478-70_478-68delinsCCA
ENST00000543245.6:c.547-70_547-68delinsCCA	ENSP00000438689.2:n.547-70_547-68delinsCCA
ENST00000577191.5:n.555-70_555-68delinsCCA
ENST00000577433.5:n.686-70_686-68delinsCCA
ENST00000577857.5:n.294-70_294-68delinsCCA
ENST00000579286.5:n.659-70_659-68delinsCCA
ENST00000579886.2:c.316-70_316-68delinsCCA	ENSP00000463246.1:n.316-70_316-68delinsCCA
ENST00000580365.1:n.209-70_209-68delinsCCA
ENST00000581378.5:c.177-51_177-49delinsCCA
ENST00000581562.5:n.524+410_524+412delinsCCA
ENST00000582166.1:n.459-70_459-68delinsCCA
ENST00000583312.5:c.478-70_478-68delinsCCA	ENSP00000467920.1:n.478-70_478-68delinsCCA
ENST00000583760.1:n.190_192delinsCCA
NM_000018.3:c.478-70_478-68delinsCCA	NP_000009.1:n.478-70_478-68delinsCCA
NM_001033859.2:c.412-70_412-68delinsCCA	NP_001029031.1:n.412-70_412-68delinsCCA
NM_001270447.1:c.547-70_547-68delinsCCA	NP_001257376.1:n.547-70_547-68delinsCCA
NM_001270448.1:c.250-70_250-68delinsCCA	NP_001257377.1:n.250-70_250-68delinsCCA
XM_006721516.2:c.478-70_478-68delinsCCA	XP_006721579.2:n.478-70_478-68delinsCCA
XM_011523829.1:c.478-70_478-68delinsCCA	XP_011522131.1:n.478-70_478-68delinsCCA
XM_011523830.1:c.478-70_478-68delinsCCA	XP_011522132.1:n.478-70_478-68delinsCCA
XR_934021.1:n.585-70_585-68delinsCCA
XR_934022.1:n.585-70_585-68delinsCCA
XR_934023.1:n.585-70_585-68delinsCCA
XM_006721516.3:c.478-70_478-68delinsCCA	XP_006721579.2:n.478-70_478-68delinsCCA
XM_011523829.2:c.478-70_478-68delinsCCA	XP_011522131.1:n.478-70_478-68delinsCCA
XM_011523830.2:c.478-70_478-68delinsCCA	XP_011522132.1:n.478-70_478-68delinsCCA
XM_024450741.1:c.478-70_478-68delinsCCA	XP_024306509.1:n.478-70_478-68delinsCCA
XR_934021.2:n.537-70_537-68delinsCCA
XR_934022.2:n.537-70_537-68delinsCCA
XR_934023.2:n.537-70_537-68delinsCCA
NM_000018.4:c.478-70_478-68delinsCCA MANE Select	NP_000009.1:n.478-70_478-68delinsCCA
NM_001033859.3:c.412-70_412-68delinsCCA	NP_001029031.1:n.412-70_412-68delinsCCA
NM_001270447.2:c.547-70_547-68delinsCCA	NP_001257376.1:n.547-70_547-68delinsCCA
NM_001270448.2:c.250-70_250-68delinsCCA	NP_001257377.1:n.250-70_250-68delinsCCA