Canonical Allele Identifier: CA397723064

Gene: ACADVL

Linked Data

• MyVariant Identifiers: chr17:g.7124889T>G (hg19) ; chr17:g.7221570T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7221570T>G , CM000679.2:g.7221570T>G	GRCh38
NC_000017.10:g.7124889T>G , CM000679.1:g.7124889T>G	GRCh37
NC_000017.9:g.7065613T>G	NCBI36
NG_007975.1:g.6737T>G
NG_008391.2:g.3481A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.510T>G MANE Select	ENSP00000349297.5:p.His170Gln
ENST00000322910.9:c.*465T>G	ENSP00000325395.5:n.*465T>G
ENST00000350303.9:c.444T>G	ENSP00000344152.5:p.His148Gln
ENST00000356839.9:c.510T>G	ENSP00000349297.5:p.His170Gln
ENST00000543245.6:c.579T>G	ENSP00000438689.2:p.His193Gln
ENST00000577191.5:n.587T>G
ENST00000577433.5:n.718T>G
ENST00000577857.5:n.326T>G
ENST00000579286.5:n.691T>G
ENST00000579886.2:c.348T>G	ENSP00000463246.1:p.His116Gln
ENST00000580365.1:n.241T>G
ENST00000581378.5:c.228T>G
ENST00000581562.5:n.525-382T>G
ENST00000582166.1:n.491T>G
ENST00000583312.5:c.510T>G	ENSP00000467920.1:p.His170Gln
ENST00000583760.1:n.292T>G
NM_000018.3:c.510T>G	NP_000009.1:p.His170Gln
NM_001033859.2:c.444T>G	NP_001029031.1:p.His148Gln
NM_001270447.1:c.579T>G	NP_001257376.1:p.His193Gln
NM_001270448.1:c.282T>G	NP_001257377.1:p.His94Gln
XM_006721516.2:c.510T>G	XP_006721579.2:p.His170Gln
XM_011523829.1:c.510T>G	XP_011522131.1:p.His170Gln
XM_011523830.1:c.510T>G	XP_011522132.1:p.His170Gln
XR_934021.1:n.617T>G
XR_934022.1:n.617T>G
XR_934023.1:n.617T>G
XM_006721516.3:c.510T>G	XP_006721579.2:p.His170Gln
XM_011523829.2:c.510T>G	XP_011522131.1:p.His170Gln
XM_011523830.2:c.510T>G	XP_011522132.1:p.His170Gln
XM_024450741.1:c.510T>G	XP_024306509.1:p.His170Gln
XR_934021.2:n.569T>G
XR_934022.2:n.569T>G
XR_934023.2:n.569T>G
NM_000018.4:c.510T>G MANE Select	NP_000009.1:p.His170Gln
NM_001033859.3:c.444T>G	NP_001029031.1:p.His148Gln
NM_001270447.2:c.579T>G	NP_001257376.1:p.His193Gln
NM_001270448.2:c.282T>G	NP_001257377.1:p.His94Gln