Canonical Allele Identifier: CA397725627

Gene: ACADVL

Linked Data

• MyVariant Identifiers: chr17:g.7127869T>G (hg19) ; chr17:g.7224550T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7224550T>G , CM000679.2:g.7224550T>G	GRCh38
NC_000017.10:g.7127869T>G , CM000679.1:g.7127869T>G	GRCh37
NC_000017.9:g.7068593T>G	NCBI36
NG_007975.1:g.9717T>G
NG_008391.2:g.501A>C
NG_033038.1:g.14995A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1676T>G MANE Select	ENSP00000349297.5:p.Val559Gly
ENST00000322910.9:c.*1631T>G	ENSP00000325395.5:n.*1631T>G
ENST00000350303.9:c.1610T>G	ENSP00000344152.5:p.Val537Gly
ENST00000356839.9:c.1676T>G	ENSP00000349297.5:p.Val559Gly
ENST00000542255.6:c.534T>G
ENST00000543245.6:c.1745T>G	ENSP00000438689.2:p.Val582Gly
ENST00000578319.5:n.257T>G
ENST00000578711.1:n.1046T>G
ENST00000578809.5:n.248T>G
ENST00000579391.1:n.280T>G
ENST00000579425.5:n.792T>G
ENST00000579546.1:c.411T>G
ENST00000582450.1:n.184T>G
ENST00000583074.5:n.297T>G
ENST00000583848.5:c.62T>G	ENSP00000466487.1:p.Val21Gly
ENST00000583850.5:n.447T>G
ENST00000583858.5:c.607T>G
ENST00000585203.6:n.867T>G
NM_000018.3:c.1676T>G	NP_000009.1:p.Val559Gly
NM_001033859.2:c.1610T>G	NP_001029031.1:p.Val537Gly
NM_001270447.1:c.1745T>G	NP_001257376.1:p.Val582Gly
NM_001270448.1:c.1448T>G	NP_001257377.1:p.Val483Gly
XM_006721516.2:c.1676T>G	XP_006721579.2:p.Val559Gly
XM_011523829.1:c.1574T>G	XP_011522131.1:p.Val525Gly
XM_011523830.1:c.1574T>G	XP_011522132.1:p.Val525Gly
XR_934021.1:n.1779T>G
XR_934022.1:n.1685T>G
XR_934023.1:n.1685T>G
XM_006721516.3:c.1676T>G	XP_006721579.2:p.Val559Gly
XM_011523829.2:c.1574T>G	XP_011522131.1:p.Val525Gly
XM_011523830.2:c.1574T>G	XP_011522132.1:p.Val525Gly
XM_024450741.1:c.1664T>G	XP_024306509.1:p.Val555Gly
XR_934021.2:n.1731T>G
XR_934022.2:n.1637T>G
XR_934023.2:n.1637T>G
NM_000018.4:c.1676T>G MANE Select	NP_000009.1:p.Val559Gly
NM_001033859.3:c.1610T>G	NP_001029031.1:p.Val537Gly
NM_001270447.2:c.1745T>G	NP_001257376.1:p.Val582Gly
NM_001270448.2:c.1448T>G	NP_001257377.1:p.Val483Gly