Canonical Allele Identifier: CA397722528

Gene: ACADVL

Linked Data

• MyVariant Identifiers: chr17:g.7124103C>A (hg19) ; chr17:g.7220784C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7220784C>A , CM000679.2:g.7220784C>A	GRCh38
NC_000017.10:g.7124103C>A , CM000679.1:g.7124103C>A	GRCh37
NC_000017.9:g.7064827C>A	NCBI36
NG_007975.1:g.5951C>A
NG_008391.2:g.4267G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.296C>A MANE Select	ENSP00000349297.5:p.Thr99Lys
ENST00000322910.9:c.*251C>A	ENSP00000325395.5:n.*251C>A
ENST00000350303.9:c.230C>A	ENSP00000344152.5:p.Thr77Lys
ENST00000356839.9:c.296C>A	ENSP00000349297.5:p.Thr99Lys
ENST00000543245.6:c.365C>A	ENSP00000438689.2:p.Thr122Lys
ENST00000577191.5:n.373C>A
ENST00000577433.5:n.504C>A
ENST00000577857.5:n.247C>A
ENST00000579286.5:n.477C>A
ENST00000579886.2:c.202-161C>A	ENSP00000463246.1:n.202-161C>A
ENST00000580365.1:n.27C>A
ENST00000581562.5:n.343C>A
ENST00000582056.5:n.386C>A
ENST00000582166.1:n.184C>A
ENST00000582356.5:n.495C>A
ENST00000583312.5:c.296C>A	ENSP00000467920.1:p.Thr99Lys
ENST00000584103.5:c.296C>A	ENSP00000465353.1:p.Thr99Lys
NM_000018.3:c.296C>A	NP_000009.1:p.Thr99Lys
NM_001033859.2:c.230C>A	NP_001029031.1:p.Thr77Lys
NM_001270447.1:c.365C>A	NP_001257376.1:p.Thr122Lys
NM_001270448.1:c.68C>A	NP_001257377.1:p.Thr23Lys
XM_006721516.2:c.296C>A	XP_006721579.2:p.Thr99Lys
XM_011523829.1:c.296C>A	XP_011522131.1:p.Thr99Lys
XM_011523830.1:c.296C>A	XP_011522132.1:p.Thr99Lys
XR_934021.1:n.403C>A
XR_934022.1:n.403C>A
XR_934023.1:n.403C>A
XM_006721516.3:c.296C>A	XP_006721579.2:p.Thr99Lys
XM_011523829.2:c.296C>A	XP_011522131.1:p.Thr99Lys
XM_011523830.2:c.296C>A	XP_011522132.1:p.Thr99Lys
XM_024450741.1:c.296C>A	XP_024306509.1:p.Thr99Lys
XR_934021.2:n.355C>A
XR_934022.2:n.355C>A
XR_934023.2:n.355C>A
NM_000018.4:c.296C>A MANE Select	NP_000009.1:p.Thr99Lys
NM_001033859.3:c.230C>A	NP_001029031.1:p.Thr77Lys
NM_001270447.2:c.365C>A	NP_001257376.1:p.Thr122Lys
NM_001270448.2:c.68C>A	NP_001257377.1:p.Thr23Lys