Canonical Allele Identifier: CA397726159

Gene: ACADVL

Linked Data

• MyVariant Identifiers: chr17:g.7128357A>G (hg19) ; chr17:g.7225038A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7225038A>G , CM000679.2:g.7225038A>G	GRCh38
NC_000017.10:g.7128357A>G , CM000679.1:g.7128357A>G	GRCh37
NC_000017.9:g.7069081A>G	NCBI36
NG_007975.1:g.10205A>G
NG_008391.2:g.13T>C
NG_033038.1:g.14507T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1909A>G MANE Select	ENSP00000349297.5:p.Ile637Val
ENST00000322910.9:c.*1864A>G	ENSP00000325395.5:n.*1864A>G
ENST00000350303.9:c.1843A>G	ENSP00000344152.5:p.Ile615Val
ENST00000356839.9:c.1909A>G	ENSP00000349297.5:p.Ile637Val
ENST00000542255.6:c.788A>G
ENST00000543245.6:c.1978A>G	ENSP00000438689.2:p.Ile660Val
ENST00000578033.1:n.334A>G
ENST00000578319.5:n.490A>G
ENST00000578711.1:n.1534A>G
ENST00000578809.5:n.481A>G
ENST00000579425.5:n.1025A>G
ENST00000583848.5:c.275A>G	ENSP00000466487.1:n.275A>G
ENST00000583850.5:n.680A>G
ENST00000583858.5:c.840A>G
NM_000018.3:c.1909A>G	NP_000009.1:p.Ile637Val
NM_001033859.2:c.1843A>G	NP_001029031.1:p.Ile615Val
NM_001270447.1:c.1978A>G	NP_001257376.1:p.Ile660Val
NM_001270448.1:c.1681A>G	NP_001257377.1:p.Ile561Val
XM_006721516.2:c.1930A>G	XP_006721579.2:p.Ile644Val
XM_011523829.1:c.1828A>G	XP_011522131.1:p.Ile610Val
XM_011523830.1:c.1807A>G	XP_011522132.1:p.Ile603Val
XR_934021.1:n.2012A>G
XR_934022.1:n.1918A>G
XR_934023.1:n.1939A>G
XM_006721516.3:c.1930A>G	XP_006721579.2:p.Ile644Val
XM_011523829.2:c.1828A>G	XP_011522131.1:p.Ile610Val
XM_011523830.2:c.1807A>G	XP_011522132.1:p.Ile603Val
XM_024450741.1:c.1897A>G	XP_024306509.1:p.Ile633Val
XR_934021.2:n.1964A>G
XR_934022.2:n.1870A>G
XR_934023.2:n.1891A>G
NM_000018.4:c.1909A>G MANE Select	NP_000009.1:p.Ile637Val
NM_001033859.3:c.1843A>G	NP_001029031.1:p.Ile615Val
NM_001270447.2:c.1978A>G	NP_001257376.1:p.Ile660Val
NM_001270448.2:c.1681A>G	NP_001257377.1:p.Ile561Val