Canonical Allele Identifier: CA397725465

Gene: ACADVL

Linked Data

• MyVariant Identifiers: chr17:g.7127710C>G (hg19) ; chr17:g.7224391C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7224391C>G , CM000679.2:g.7224391C>G	GRCh38
NC_000017.10:g.7127710C>G , CM000679.1:g.7127710C>G	GRCh37
NC_000017.9:g.7068434C>G	NCBI36
NG_007975.1:g.9558C>G
NG_008391.2:g.660G>C
NG_033038.1:g.15154G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1603C>G MANE Select	ENSP00000349297.5:p.Leu535Val
ENST00000322910.9:c.*1558C>G	ENSP00000325395.5:n.*1558C>G
ENST00000350303.9:c.1537C>G	ENSP00000344152.5:p.Leu513Val
ENST00000356839.9:c.1603C>G	ENSP00000349297.5:p.Leu535Val
ENST00000542255.6:c.461C>G
ENST00000543245.6:c.1672C>G	ENSP00000438689.2:p.Leu558Val
ENST00000578319.5:n.98C>G
ENST00000578711.1:n.887C>G
ENST00000578809.5:n.175C>G
ENST00000579391.1:n.211C>G
ENST00000579425.5:n.719C>G
ENST00000579546.1:c.342C>G
ENST00000579894.5:n.390C>G
ENST00000582450.1:n.111C>G
ENST00000583074.5:n.224C>G
ENST00000583850.5:n.378C>G
ENST00000583858.5:c.534C>G
ENST00000585203.6:n.794C>G
NM_000018.3:c.1603C>G	NP_000009.1:p.Leu535Val
NM_001033859.2:c.1537C>G	NP_001029031.1:p.Leu513Val
NM_001270447.1:c.1672C>G	NP_001257376.1:p.Leu558Val
NM_001270448.1:c.1375C>G	NP_001257377.1:p.Leu459Val
XM_006721516.2:c.1603C>G	XP_006721579.2:p.Leu535Val
XM_011523829.1:c.1505C>G	XP_011522131.1:p.Ala502Gly
XM_011523830.1:c.1505C>G	XP_011522132.1:p.Ala502Gly
XR_934021.1:n.1710C>G
XR_934022.1:n.1612C>G
XR_934023.1:n.1612C>G
XM_006721516.3:c.1603C>G	XP_006721579.2:p.Leu535Val
XM_011523829.2:c.1505C>G	XP_011522131.1:p.Ala502Gly
XM_011523830.2:c.1505C>G	XP_011522132.1:p.Ala502Gly
XM_024450741.1:c.1505C>G	XP_024306509.1:p.Ala502Gly
XR_934021.2:n.1662C>G
XR_934022.2:n.1564C>G
XR_934023.2:n.1564C>G
NM_000018.4:c.1603C>G MANE Select	NP_000009.1:p.Leu535Val
NM_001033859.3:c.1537C>G	NP_001029031.1:p.Leu513Val
NM_001270447.2:c.1672C>G	NP_001257376.1:p.Leu558Val
NM_001270448.2:c.1375C>G	NP_001257377.1:p.Leu459Val