Canonical Allele Identifier: CA397723145

Gene: ACADVL

Linked Data

• MyVariant Identifiers: chr17:g.7124929A>T (hg19) ; chr17:g.7221610A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7221610A>T , CM000679.2:g.7221610A>T	GRCh38
NC_000017.10:g.7124929A>T , CM000679.1:g.7124929A>T	GRCh37
NC_000017.9:g.7065653A>T	NCBI36
NG_007975.1:g.6777A>T
NG_008391.2:g.3441T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000356839.10:c.550A>T MANE Select	ENSP00000349297.5:p.Ile184Phe
ENST00000322910.9:c.*505A>T	ENSP00000325395.5:n.*505A>T
ENST00000350303.9:c.484A>T	ENSP00000344152.5:p.Ile162Phe
ENST00000356839.9:c.550A>T	ENSP00000349297.5:p.Ile184Phe
ENST00000543245.6:c.619A>T	ENSP00000438689.2:p.Ile207Phe
ENST00000577191.5:n.627A>T
ENST00000577433.5:n.758A>T
ENST00000577857.5:n.366A>T
ENST00000579286.5:n.731A>T
ENST00000579886.2:c.388A>T	ENSP00000463246.1:p.Ile130Phe
ENST00000580365.1:n.281A>T
ENST00000581378.5:c.268A>T
ENST00000581562.5:n.525-342A>T
ENST00000582166.1:n.531A>T
ENST00000583312.5:c.550A>T	ENSP00000467920.1:p.Ile184Phe
ENST00000583760.1:n.332A>T
NM_000018.3:c.550A>T	NP_000009.1:p.Ile184Phe
NM_001033859.2:c.484A>T	NP_001029031.1:p.Ile162Phe
NM_001270447.1:c.619A>T	NP_001257376.1:p.Ile207Phe
NM_001270448.1:c.322A>T	NP_001257377.1:p.Ile108Phe
XM_006721516.2:c.550A>T	XP_006721579.2:p.Ile184Phe
XM_011523829.1:c.550A>T	XP_011522131.1:p.Ile184Phe
XM_011523830.1:c.550A>T	XP_011522132.1:p.Ile184Phe
XR_934021.1:n.657A>T
XR_934022.1:n.657A>T
XR_934023.1:n.657A>T
XM_006721516.3:c.550A>T	XP_006721579.2:p.Ile184Phe
XM_011523829.2:c.550A>T	XP_011522131.1:p.Ile184Phe
XM_011523830.2:c.550A>T	XP_011522132.1:p.Ile184Phe
XM_024450741.1:c.550A>T	XP_024306509.1:p.Ile184Phe
XR_934021.2:n.609A>T
XR_934022.2:n.609A>T
XR_934023.2:n.609A>T
NM_000018.4:c.550A>T MANE Select	NP_000009.1:p.Ile184Phe
NM_001033859.3:c.484A>T	NP_001029031.1:p.Ile162Phe
NM_001270447.2:c.619A>T	NP_001257376.1:p.Ile207Phe
NM_001270448.2:c.322A>T	NP_001257377.1:p.Ile108Phe