Canonical Allele Identifier: CA497693945

Gene: ACADVL

Linked Data

• MyVariant Identifiers: chr17:g.7124086G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7220767G>T , CM000679.2:g.7220767G>T	GRCh38
NC_000017.10:g.7124086G>T , CM000679.1:g.7124086G>T	GRCh37
NC_000017.9:g.7064810G>T	NCBI36
NG_007975.1:g.5934G>T
NG_008391.2:g.4284C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.279G>T MANE Select	ENSP00000349297.5:p.Val93=
ENST00000322910.9:c.*234G>T	ENSP00000325395.5:n.*234G>T
ENST00000350303.9:c.213G>T	ENSP00000344152.5:p.Val71=
ENST00000356839.9:c.279G>T	ENSP00000349297.5:p.Val93=
ENST00000543245.6:c.348G>T	ENSP00000438689.2:p.Val116=
ENST00000577191.5:n.356G>T
ENST00000577433.5:n.487G>T
ENST00000577857.5:n.230G>T
ENST00000579286.5:n.460G>T
ENST00000579886.2:c.202-178G>T	ENSP00000463246.1:n.202-178G>T
ENST00000580263.5:n.532G>T
ENST00000580365.1:n.10G>T
ENST00000581562.5:n.326G>T
ENST00000582056.5:n.369G>T
ENST00000582166.1:n.167G>T
ENST00000582356.5:n.478G>T
ENST00000583312.5:c.279G>T	ENSP00000467920.1:p.Val93=
ENST00000584103.5:c.279G>T	ENSP00000465353.1:p.Val93=
NM_000018.3:c.279G>T	NP_000009.1:p.Val93=
NM_001033859.2:c.213G>T	NP_001029031.1:p.Val71=
NM_001270447.1:c.348G>T	NP_001257376.1:p.Val116=
NM_001270448.1:c.51G>T	NP_001257377.1:p.Val17=
XM_006721516.2:c.279G>T	XP_006721579.2:p.Val93=
XM_011523829.1:c.279G>T	XP_011522131.1:p.Val93=
XM_011523830.1:c.279G>T	XP_011522132.1:p.Val93=
XR_934021.1:n.386G>T
XR_934022.1:n.386G>T
XR_934023.1:n.386G>T
XM_006721516.3:c.279G>T	XP_006721579.2:p.Val93=
XM_011523829.2:c.279G>T	XP_011522131.1:p.Val93=
XM_011523830.2:c.279G>T	XP_011522132.1:p.Val93=
XM_024450741.1:c.279G>T	XP_024306509.1:p.Val93=
XR_934021.2:n.338G>T
XR_934022.2:n.338G>T
XR_934023.2:n.338G>T
NM_000018.4:c.279G>T MANE Select	NP_000009.1:p.Val93=
NM_001033859.3:c.213G>T	NP_001029031.1:p.Val71=
NM_001270447.2:c.348G>T	NP_001257376.1:p.Val116=
NM_001270448.2:c.51G>T	NP_001257377.1:p.Val17=