Canonical Allele Identifier: CA397725049

Gene: ACADVL

Linked Data

• MyVariant Identifiers: chr17:g.7127362C>A (hg19) ; chr17:g.7224043C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7224043C>A , CM000679.2:g.7224043C>A	GRCh38
NC_000017.10:g.7127362C>A , CM000679.1:g.7127362C>A	GRCh37
NC_000017.9:g.7068086C>A	NCBI36
NG_007975.1:g.9210C>A
NG_008391.2:g.1008G>T
NG_033038.1:g.15502G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000356839.10:c.1408C>A MANE Select	ENSP00000349297.5:p.Leu470Met
ENST00000322910.9:c.*1363C>A	ENSP00000325395.5:n.*1363C>A
ENST00000350303.9:c.1342C>A	ENSP00000344152.5:p.Leu448Met
ENST00000356839.9:c.1408C>A	ENSP00000349297.5:p.Leu470Met
ENST00000542255.6:c.266C>A
ENST00000543245.6:c.1477C>A	ENSP00000438689.2:p.Leu493Met
ENST00000578711.1:n.539C>A
ENST00000579425.5:n.524C>A
ENST00000579546.1:c.245C>A
ENST00000579894.5:n.119C>A
ENST00000583074.5:n.127C>A
ENST00000583850.5:n.183C>A
ENST00000583858.5:c.437C>A
ENST00000585203.6:n.599C>A
NM_000018.3:c.1408C>A	NP_000009.1:p.Leu470Met
NM_001033859.2:c.1342C>A	NP_001029031.1:p.Leu448Met
NM_001270447.1:c.1477C>A	NP_001257376.1:p.Leu493Met
NM_001270448.1:c.1180C>A	NP_001257377.1:p.Leu394Met
XM_006721516.2:c.1408C>A	XP_006721579.2:p.Leu470Met
XM_011523829.1:c.1408C>A	XP_011522131.1:p.Leu470Met
XM_011523830.1:c.1408C>A	XP_011522132.1:p.Leu470Met
XR_934021.1:n.1515C>A
XR_934022.1:n.1515C>A
XR_934023.1:n.1515C>A
XM_006721516.3:c.1408C>A	XP_006721579.2:p.Leu470Met
XM_011523829.2:c.1408C>A	XP_011522131.1:p.Leu470Met
XM_011523830.2:c.1408C>A	XP_011522132.1:p.Leu470Met
XM_024450741.1:c.1408C>A	XP_024306509.1:p.Leu470Met
XR_934021.2:n.1467C>A
XR_934022.2:n.1467C>A
XR_934023.2:n.1467C>A
NM_000018.4:c.1408C>A MANE Select	NP_000009.1:p.Leu470Met
NM_001033859.3:c.1342C>A	NP_001029031.1:p.Leu448Met
NM_001270447.2:c.1477C>A	NP_001257376.1:p.Leu493Met
NM_001270448.2:c.1180C>A	NP_001257377.1:p.Leu394Met