Canonical Allele Identifier: CA2245699834

Gene: ACADVL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7221442_7221449delinsCCCTAGGT , CM000679.2:g.7221442_7221449delinsCCCTAGGT	GRCh38
NC_000017.10:g.7124761_7124768delinsCCCTAGGT , CM000679.1:g.7124761_7124768delinsCCCTAGGT	GRCh37
NC_000017.9:g.7065485_7065492delinsCCCTAGGT	NCBI36
NG_007975.1:g.6609_6616delinsCCCTAGGT
NG_008391.2:g.3602_3609delinsACCTAGGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000356839.10:c.478-96_478-89delinsCCCTAGGT MANE Select	ENSP00000349297.5:n.478-96_478-89delinsCC...
ENST00000322910.9:c.*433-96_*433-89delinsCCCTAGGT	ENSP00000325395.5:n.*433-96_*433-89delins...
ENST00000350303.9:c.412-96_412-89delinsCCCTAGGT	ENSP00000344152.5:n.412-96_412-89delinsCC...
ENST00000356839.9:c.478-96_478-89delinsCCCTAGGT	ENSP00000349297.5:n.478-96_478-89delinsCC...
ENST00000543245.6:c.547-96_547-89delinsCCCTAGGT	ENSP00000438689.2:n.547-96_547-89delinsCC...
ENST00000577191.5:n.555-96_555-89delinsCCCTAGGT
ENST00000577433.5:n.686-96_686-89delinsCCCTAGGT
ENST00000577857.5:n.294-96_294-89delinsCCCTAGGT
ENST00000579286.5:n.659-96_659-89delinsCCCTAGGT
ENST00000579886.2:c.316-96_316-89delinsCCCTAGGT	ENSP00000463246.1:n.316-96_316-89delinsCC...
ENST00000580365.1:n.209-96_209-89delinsCCCTAGGT
ENST00000581378.5:c.177-77_177-70delinsCCCTAGGT
ENST00000581562.5:n.524+384_524+391delinsCCCTAGGT
ENST00000582166.1:n.459-96_459-89delinsCCCTAGGT
ENST00000583312.5:c.478-96_478-89delinsCCCTAGGT	ENSP00000467920.1:n.478-96_478-89delinsCC...
ENST00000583760.1:n.164_171delinsCCCTAGGT
NM_000018.3:c.478-96_478-89delinsCCCTAGGT	NP_000009.1:n.478-96_478-89delinsCCCTAGGT...
NM_001033859.2:c.412-96_412-89delinsCCCTAGGT	NP_001029031.1:n.412-96_412-89delinsCCCTA...
NM_001270447.1:c.547-96_547-89delinsCCCTAGGT	NP_001257376.1:n.547-96_547-89delinsCCCTA...
NM_001270448.1:c.250-96_250-89delinsCCCTAGGT	NP_001257377.1:n.250-96_250-89delinsCCCTA...
XM_006721516.2:c.478-96_478-89delinsCCCTAGGT	XP_006721579.2:n.478-96_478-89delinsCCCTA...
XM_011523829.1:c.478-96_478-89delinsCCCTAGGT	XP_011522131.1:n.478-96_478-89delinsCCCTA...
XM_011523830.1:c.478-96_478-89delinsCCCTAGGT	XP_011522132.1:n.478-96_478-89delinsCCCTA...
XR_934021.1:n.585-96_585-89delinsCCCTAGGT
XR_934022.1:n.585-96_585-89delinsCCCTAGGT
XR_934023.1:n.585-96_585-89delinsCCCTAGGT
XM_006721516.3:c.478-96_478-89delinsCCCTAGGT	XP_006721579.2:n.478-96_478-89delinsCCCTA...
XM_011523829.2:c.478-96_478-89delinsCCCTAGGT	XP_011522131.1:n.478-96_478-89delinsCCCTA...
XM_011523830.2:c.478-96_478-89delinsCCCTAGGT	XP_011522132.1:n.478-96_478-89delinsCCCTA...
XM_024450741.1:c.478-96_478-89delinsCCCTAGGT	XP_024306509.1:n.478-96_478-89delinsCCCTA...
XR_934021.2:n.537-96_537-89delinsCCCTAGGT
XR_934022.2:n.537-96_537-89delinsCCCTAGGT
XR_934023.2:n.537-96_537-89delinsCCCTAGGT
NM_000018.4:c.478-96_478-89delinsCCCTAGGT MANE Select	NP_000009.1:n.478-96_478-89delinsCCCTAGGT...
NM_001033859.3:c.412-96_412-89delinsCCCTAGGT	NP_001029031.1:n.412-96_412-89delinsCCCTA...
NM_001270447.2:c.547-96_547-89delinsCCCTAGGT	NP_001257376.1:n.547-96_547-89delinsCCCTA...
NM_001270448.2:c.250-96_250-89delinsCCCTAGGT	NP_001257377.1:n.250-96_250-89delinsCCCTA...