Canonical Allele Identifier: CA397722312

Gene: ACADVL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7220530G>T , CM000679.2:g.7220530G>T	GRCh38
NC_000017.10:g.7123849G>T , CM000679.1:g.7123849G>T	GRCh37
NC_000017.9:g.7064573G>T	NCBI36
NG_007975.1:g.5697G>T
NG_008391.2:g.4521C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000018.4:c.204+1G>T MANE Select	NP_000009.1:n.204+1G>T
ENST00000356839.10:c.204+1G>T MANE Select	ENSP00000349297.5:n.204+1G>T
NM_000018.3:c.204+1G>T	NP_000009.1:n.204+1G>T
NM_001033859.2:c.139-74G>T	NP_001029031.1:n.139-74G>T
NM_001033859.3:c.139-74G>T	NP_001029031.1:n.139-74G>T
NM_001270447.1:c.273+1G>T	NP_001257376.1:n.273+1G>T
NM_001270447.2:c.273+1G>T	NP_001257376.1:n.273+1G>T
NM_001270448.1:c.-25+1G>T	NP_001257377.1:n.-25+1G>T
NM_001270448.2:c.-25+1G>T	NP_001257377.1:n.-25+1G>T
ENST00000322910.9:c.*159+1G>T	ENSP00000325395.5:n.*159+1G>T
ENST00000350303.9:c.139-74G>T	ENSP00000344152.5:n.139-74G>T
ENST00000356839.9:c.204+1G>T	ENSP00000349297.5:n.204+1G>T
ENST00000543245.6:c.273+1G>T	ENSP00000438689.2:n.273+1G>T
ENST00000577191.5:n.281+1G>T
ENST00000577433.5:n.339G>T
ENST00000577857.5:n.229-236G>T
ENST00000578269.5:n.578G>T
ENST00000578421.1:n.339G>T
ENST00000579286.5:n.312G>T
ENST00000579886.2:c.201+4G>T	ENSP00000463246.1:n.201+4G>T
ENST00000580263.5:n.295G>T
ENST00000581562.5:n.251+1G>T
ENST00000582056.5:n.294+1G>T
ENST00000582166.1:n.92+1G>T
ENST00000582356.5:n.330G>T
ENST00000583312.5:c.204+1G>T	ENSP00000467920.1:n.204+1G>T
ENST00000584103.5:c.204+1G>T	ENSP00000465353.1:n.204+1G>T
XM_006721516.2:c.204+1G>T	XP_006721579.2:n.204+1G>T
XM_006721516.3:c.204+1G>T	XP_006721579.2:n.204+1G>T
XM_011523829.1:c.204+1G>T	XP_011522131.1:n.204+1G>T
XM_011523829.2:c.204+1G>T	XP_011522131.1:n.204+1G>T
XM_011523830.1:c.204+1G>T	XP_011522132.1:n.204+1G>T
XM_011523830.2:c.204+1G>T	XP_011522132.1:n.204+1G>T
XM_024450741.1:c.204+1G>T	XP_024306509.1:n.204+1G>T
XR_934021.1:n.311+1G>T
XR_934021.2:n.263+1G>T
XR_934022.1:n.311+1G>T
XR_934022.2:n.263+1G>T
XR_934023.1:n.311+1G>T
XR_934023.2:n.263+1G>T