Canonical Allele Identifier: CA2245699755

Gene: ACADVL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7221414_7221415delinsGT , CM000679.2:g.7221414_7221415delinsGT	GRCh38
NC_000017.10:g.7124733_7124734delinsGT , CM000679.1:g.7124733_7124734delinsGT	GRCh37
NC_000017.9:g.7065457_7065458delinsGT	NCBI36
NG_007975.1:g.6581_6582delinsGT
NG_008391.2:g.3636_3637delinsAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000356839.10:c.478-124_478-123delinsGT MANE Select	ENSP00000349297.5:n.478-124_478-123delins...
ENST00000322910.9:c.*433-124_*433-123delinsGT	ENSP00000325395.5:n.*433-124_*433-123deli...
ENST00000350303.9:c.412-124_412-123delinsGT	ENSP00000344152.5:n.412-124_412-123delins...
ENST00000356839.9:c.478-124_478-123delinsGT	ENSP00000349297.5:n.478-124_478-123delins...
ENST00000543245.6:c.547-124_547-123delinsGT	ENSP00000438689.2:n.547-124_547-123delins...
ENST00000577191.5:n.555-124_555-123delinsGT
ENST00000577433.5:n.686-124_686-123delinsGT
ENST00000577857.5:n.294-124_294-123delinsGT
ENST00000579286.5:n.659-124_659-123delinsGT
ENST00000579886.2:c.316-124_316-123delinsGT	ENSP00000463246.1:n.316-124_316-123delins...
ENST00000580365.1:n.209-124_209-123delinsGT
ENST00000581378.5:c.177-105_177-104delinsGT
ENST00000581562.5:n.524+356_524+357delinsGT
ENST00000582166.1:n.459-124_459-123delinsGT
ENST00000583312.5:c.478-124_478-123delinsGT	ENSP00000467920.1:n.478-124_478-123delins...
ENST00000583760.1:n.136_137delinsGT
NM_000018.3:c.478-124_478-123delinsGT	NP_000009.1:n.478-124_478-123delinsGT
NM_001033859.2:c.412-124_412-123delinsGT	NP_001029031.1:n.412-124_412-123delinsGT
NM_001270447.1:c.547-124_547-123delinsGT	NP_001257376.1:n.547-124_547-123delinsGT
NM_001270448.1:c.250-124_250-123delinsGT	NP_001257377.1:n.250-124_250-123delinsGT
XM_006721516.2:c.478-124_478-123delinsGT	XP_006721579.2:n.478-124_478-123delinsGT
XM_011523829.1:c.478-124_478-123delinsGT	XP_011522131.1:n.478-124_478-123delinsGT
XM_011523830.1:c.478-124_478-123delinsGT	XP_011522132.1:n.478-124_478-123delinsGT
XR_934021.1:n.585-124_585-123delinsGT
XR_934022.1:n.585-124_585-123delinsGT
XR_934023.1:n.585-124_585-123delinsGT
XM_006721516.3:c.478-124_478-123delinsGT	XP_006721579.2:n.478-124_478-123delinsGT
XM_011523829.2:c.478-124_478-123delinsGT	XP_011522131.1:n.478-124_478-123delinsGT
XM_011523830.2:c.478-124_478-123delinsGT	XP_011522132.1:n.478-124_478-123delinsGT
XM_024450741.1:c.478-124_478-123delinsGT	XP_024306509.1:n.478-124_478-123delinsGT
XR_934021.2:n.537-124_537-123delinsGT
XR_934022.2:n.537-124_537-123delinsGT
XR_934023.2:n.537-124_537-123delinsGT
NM_000018.4:c.478-124_478-123delinsGT MANE Select	NP_000009.1:n.478-124_478-123delinsGT
NM_001033859.3:c.412-124_412-123delinsGT	NP_001029031.1:n.412-124_412-123delinsGT
NM_001270447.2:c.547-124_547-123delinsGT	NP_001257376.1:n.547-124_547-123delinsGT
NM_001270448.2:c.250-124_250-123delinsGT	NP_001257377.1:n.250-124_250-123delinsGT