Canonical Allele Identifier: CA2245698827

Gene: ACADVL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7220726_7220740delinsGCCAGCCTGGCCTGA , CM000679.2:g.7220726_7220740delinsGCCAGCCTGGCCTGA	GRCh38
NC_000017.10:g.7124045_7124059delinsGCCAGCCTGGCCTGA , CM000679.1:g.7124045_7124059delinsGCCAGCCTGGCCTGA	GRCh37
NC_000017.9:g.7064769_7064783delinsGCCAGCCTGGCCTGA	NCBI36
NG_007975.1:g.5893_5907delinsGCCAGCCTGGCCTGA
NG_008391.2:g.4311_4325delinsTCAGGCCAGGCTGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.278-40_278-26delinsGCCAGCCTGGCCTGA MANE Select	ENSP00000349297.5:n.278-40_278-26delinsGCCAGCCTGGCCTGA
ENST00000322910.9:c.*233-40_*233-26delinsGCCAGCCTGGCCTGA	ENSP00000325395.5:n.*233-40_*233-26delinsGCCAGCCTGGCCTGA
ENST00000350303.9:c.212-40_212-26delinsGCCAGCCTGGCCTGA	ENSP00000344152.5:n.212-40_212-26delinsGCCAGCCTGGCCTGA
ENST00000356839.9:c.278-40_278-26delinsGCCAGCCTGGCCTGA	ENSP00000349297.5:n.278-40_278-26delinsGCCAGCCTGGCCTGA
ENST00000543245.6:c.347-40_347-26delinsGCCAGCCTGGCCTGA	ENSP00000438689.2:n.347-40_347-26delinsGCCAGCCTGGCCTGA
ENST00000577191.5:n.355-40_355-26delinsGCCAGCCTGGCCTGA
ENST00000577433.5:n.486-40_486-26delinsGCCAGCCTGGCCTGA
ENST00000577857.5:n.229-40_229-26delinsGCCAGCCTGGCCTGA
ENST00000579286.5:n.459-40_459-26delinsGCCAGCCTGGCCTGA
ENST00000579886.2:c.201+200_202-205delinsGCCAGCCTGGCCTGA	ENSP00000463246.1:n.201+200_202-205delinsGCCAGCCTGGCCTGA
ENST00000580263.5:n.491_505delinsGCCAGCCTGGCCTGA
ENST00000581562.5:n.325-40_325-26delinsGCCAGCCTGGCCTGA
ENST00000582056.5:n.368-40_368-26delinsGCCAGCCTGGCCTGA
ENST00000582166.1:n.166-40_166-26delinsGCCAGCCTGGCCTGA
ENST00000582356.5:n.477-40_477-26delinsGCCAGCCTGGCCTGA
ENST00000583312.5:c.278-40_278-26delinsGCCAGCCTGGCCTGA	ENSP00000467920.1:n.278-40_278-26delinsGCCAGCCTGGCCTGA
ENST00000584103.5:c.278-40_278-26delinsGCCAGCCTGGCCTGA	ENSP00000465353.1:n.278-40_278-26delinsGCCAGCCTGGCCTGA
NM_000018.3:c.278-40_278-26delinsGCCAGCCTGGCCTGA	NP_000009.1:n.278-40_278-26delinsGCCAGCCTGGCCTGA
NM_001033859.2:c.212-40_212-26delinsGCCAGCCTGGCCTGA	NP_001029031.1:n.212-40_212-26delinsGCCAGCCTGGCCTGA
NM_001270447.1:c.347-40_347-26delinsGCCAGCCTGGCCTGA	NP_001257376.1:n.347-40_347-26delinsGCCAGCCTGGCCTGA
NM_001270448.1:c.50-40_50-26delinsGCCAGCCTGGCCTGA	NP_001257377.1:n.50-40_50-26delinsGCCAGCCTGGCCTGA
XM_006721516.2:c.278-40_278-26delinsGCCAGCCTGGCCTGA	XP_006721579.2:n.278-40_278-26delinsGCCAGCCTGGCCTGA
XM_011523829.1:c.278-40_278-26delinsGCCAGCCTGGCCTGA	XP_011522131.1:n.278-40_278-26delinsGCCAGCCTGGCCTGA
XM_011523830.1:c.278-40_278-26delinsGCCAGCCTGGCCTGA	XP_011522132.1:n.278-40_278-26delinsGCCAGCCTGGCCTGA
XR_934021.1:n.385-40_385-26delinsGCCAGCCTGGCCTGA
XR_934022.1:n.385-40_385-26delinsGCCAGCCTGGCCTGA
XR_934023.1:n.385-40_385-26delinsGCCAGCCTGGCCTGA
XM_006721516.3:c.278-40_278-26delinsGCCAGCCTGGCCTGA	XP_006721579.2:n.278-40_278-26delinsGCCAGCCTGGCCTGA
XM_011523829.2:c.278-40_278-26delinsGCCAGCCTGGCCTGA	XP_011522131.1:n.278-40_278-26delinsGCCAGCCTGGCCTGA
XM_011523830.2:c.278-40_278-26delinsGCCAGCCTGGCCTGA	XP_011522132.1:n.278-40_278-26delinsGCCAGCCTGGCCTGA
XM_024450741.1:c.278-40_278-26delinsGCCAGCCTGGCCTGA	XP_024306509.1:n.278-40_278-26delinsGCCAGCCTGGCCTGA
XR_934021.2:n.337-40_337-26delinsGCCAGCCTGGCCTGA
XR_934022.2:n.337-40_337-26delinsGCCAGCCTGGCCTGA
XR_934023.2:n.337-40_337-26delinsGCCAGCCTGGCCTGA
NM_000018.4:c.278-40_278-26delinsGCCAGCCTGGCCTGA MANE Select	NP_000009.1:n.278-40_278-26delinsGCCAGCCTGGCCTGA
NM_001033859.3:c.212-40_212-26delinsGCCAGCCTGGCCTGA	NP_001029031.1:n.212-40_212-26delinsGCCAGCCTGGCCTGA
NM_001270447.2:c.347-40_347-26delinsGCCAGCCTGGCCTGA	NP_001257376.1:n.347-40_347-26delinsGCCAGCCTGGCCTGA
NM_001270448.2:c.50-40_50-26delinsGCCAGCCTGGCCTGA	NP_001257377.1:n.50-40_50-26delinsGCCAGCCTGGCCTGA