Canonical Allele Identifier: CA397722321

Gene: ACADVL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7220603G>C , CM000679.2:g.7220603G>C	GRCh38
NC_000017.10:g.7123922G>C , CM000679.1:g.7123922G>C	GRCh37
NC_000017.9:g.7064646G>C	NCBI36
NG_007975.1:g.5770G>C
NG_008391.2:g.4448C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000018.4:c.205-1G>C MANE Select	NP_000009.1:n.205-1G>C
ENST00000356839.10:c.205-1G>C MANE Select	ENSP00000349297.5:n.205-1G>C
NM_000018.3:c.205-1G>C	NP_000009.1:n.205-1G>C
NM_001033859.2:c.139-1G>C	NP_001029031.1:n.139-1G>C
NM_001033859.3:c.139-1G>C	NP_001029031.1:n.139-1G>C
NM_001270447.1:c.274-1G>C	NP_001257376.1:n.274-1G>C
NM_001270447.2:c.274-1G>C	NP_001257376.1:n.274-1G>C
NM_001270448.1:c.-24-1G>C	NP_001257377.1:n.-24-1G>C
NM_001270448.2:c.-24-1G>C	NP_001257377.1:n.-24-1G>C
ENST00000322910.9:c.*160-1G>C	ENSP00000325395.5:n.*160-1G>C
ENST00000350303.9:c.139-1G>C	ENSP00000344152.5:n.139-1G>C
ENST00000356839.9:c.205-1G>C	ENSP00000349297.5:n.205-1G>C
ENST00000543245.6:c.274-1G>C	ENSP00000438689.2:n.274-1G>C
ENST00000577191.5:n.282-1G>C
ENST00000577433.5:n.412G>C
ENST00000577857.5:n.229-163G>C
ENST00000578269.5:n.651G>C
ENST00000578421.1:n.412G>C
ENST00000579286.5:n.385G>C
ENST00000579886.2:c.201+77G>C	ENSP00000463246.1:n.201+77G>C
ENST00000580263.5:n.368G>C
ENST00000581562.5:n.252-1G>C
ENST00000582056.5:n.295-1G>C
ENST00000582166.1:n.93-1G>C
ENST00000582356.5:n.403G>C
ENST00000583312.5:c.205-1G>C	ENSP00000467920.1:n.205-1G>C
ENST00000584103.5:c.205-1G>C	ENSP00000465353.1:n.205-1G>C
XM_006721516.2:c.205-1G>C	XP_006721579.2:n.205-1G>C
XM_006721516.3:c.205-1G>C	XP_006721579.2:n.205-1G>C
XM_011523829.1:c.205-1G>C	XP_011522131.1:n.205-1G>C
XM_011523829.2:c.205-1G>C	XP_011522131.1:n.205-1G>C
XM_011523830.1:c.205-1G>C	XP_011522132.1:n.205-1G>C
XM_011523830.2:c.205-1G>C	XP_011522132.1:n.205-1G>C
XM_024450741.1:c.205-1G>C	XP_024306509.1:n.205-1G>C
XR_934021.1:n.312-1G>C
XR_934021.2:n.264-1G>C
XR_934022.1:n.312-1G>C
XR_934022.2:n.264-1G>C
XR_934023.1:n.312-1G>C
XR_934023.2:n.264-1G>C