Canonical Allele Identifier: CA397724744

Gene: ACADVL

Linked Data

• MyVariant Identifiers: chr17:g.7127132G>C (hg19) ; chr17:g.7223813G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7223813G>C , CM000679.2:g.7223813G>C	GRCh38
NC_000017.10:g.7127132G>C , CM000679.1:g.7127132G>C	GRCh37
NC_000017.9:g.7067856G>C	NCBI36
NG_007975.1:g.8980G>C
NG_008391.2:g.1238C>G
NG_033038.1:g.15732C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1270G>C MANE Select	ENSP00000349297.5:p.Glu424Gln
ENST00000322910.9:c.*1225G>C	ENSP00000325395.5:n.*1225G>C
ENST00000350303.9:c.1204G>C	ENSP00000344152.5:p.Glu402Gln
ENST00000356839.9:c.1270G>C	ENSP00000349297.5:p.Glu424Gln
ENST00000542255.6:c.128G>C
ENST00000543245.6:c.1339G>C	ENSP00000438689.2:p.Glu447Gln
ENST00000578579.2:n.441G>C
ENST00000578711.1:n.309G>C
ENST00000578824.5:n.686G>C
ENST00000579425.5:n.294G>C
ENST00000579546.1:c.107G>C
ENST00000583850.5:n.45G>C
ENST00000583858.5:c.299G>C
ENST00000585203.6:n.478G>C
NM_000018.3:c.1270G>C	NP_000009.1:p.Glu424Gln
NM_001033859.2:c.1204G>C	NP_001029031.1:p.Glu402Gln
NM_001270447.1:c.1339G>C	NP_001257376.1:p.Glu447Gln
NM_001270448.1:c.1042G>C	NP_001257377.1:p.Glu348Gln
XM_006721516.2:c.1270G>C	XP_006721579.2:p.Glu424Gln
XM_011523829.1:c.1270G>C	XP_011522131.1:p.Glu424Gln
XM_011523830.1:c.1270G>C	XP_011522132.1:p.Glu424Gln
XR_934021.1:n.1377G>C
XR_934022.1:n.1377G>C
XR_934023.1:n.1377G>C
XM_006721516.3:c.1270G>C	XP_006721579.2:p.Glu424Gln
XM_011523829.2:c.1270G>C	XP_011522131.1:p.Glu424Gln
XM_011523830.2:c.1270G>C	XP_011522132.1:p.Glu424Gln
XM_024450741.1:c.1270G>C	XP_024306509.1:p.Glu424Gln
XR_934021.2:n.1329G>C
XR_934022.2:n.1329G>C
XR_934023.2:n.1329G>C
NM_000018.4:c.1270G>C MANE Select	NP_000009.1:p.Glu424Gln
NM_001033859.3:c.1204G>C	NP_001029031.1:p.Glu402Gln
NM_001270447.2:c.1339G>C	NP_001257376.1:p.Glu447Gln
NM_001270448.2:c.1042G>C	NP_001257377.1:p.Glu348Gln