Canonical Allele Identifier: CA397725136

Gene: ACADVL

Linked Data

• MyVariant Identifiers: chr17:g.7127471G>T (hg19) ; chr17:g.7224152G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7224152G>T , CM000679.2:g.7224152G>T	GRCh38
NC_000017.10:g.7127471G>T , CM000679.1:g.7127471G>T	GRCh37
NC_000017.9:g.7068195G>T	NCBI36
NG_007975.1:g.9319G>T
NG_008391.2:g.899C>A
NG_033038.1:g.15393C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000356839.10:c.1441G>T MANE Select	ENSP00000349297.5:p.Gly481Ter
ENST00000322910.9:c.*1396G>T	ENSP00000325395.5:n.*1396G>T
ENST00000350303.9:c.1375G>T	ENSP00000344152.5:p.Gly459Ter
ENST00000356839.9:c.1441G>T	ENSP00000349297.5:p.Gly481Ter
ENST00000542255.6:c.299G>T
ENST00000543245.6:c.1510G>T	ENSP00000438689.2:p.Gly504Ter
ENST00000578711.1:n.648G>T
ENST00000579391.1:n.49G>T
ENST00000579425.5:n.557G>T
ENST00000579546.1:c.271+83G>T
ENST00000579894.5:n.228G>T
ENST00000583074.5:n.153+83G>T
ENST00000583850.5:n.216G>T
ENST00000583858.5:c.463+83G>T
ENST00000585203.6:n.632G>T
NM_000018.3:c.1441G>T	NP_000009.1:p.Gly481Ter
NM_001033859.2:c.1375G>T	NP_001029031.1:p.Gly459Ter
NM_001270447.1:c.1510G>T	NP_001257376.1:p.Gly504Ter
NM_001270448.1:c.1213G>T	NP_001257377.1:p.Gly405Ter
XM_006721516.2:c.1441G>T	XP_006721579.2:p.Gly481Ter
XM_011523829.1:c.1434+83G>T	XP_011522131.1:n.1434+83G>T
XM_011523830.1:c.1434+83G>T	XP_011522132.1:n.1434+83G>T
XR_934021.1:n.1548G>T
XR_934022.1:n.1541+83G>T
XR_934023.1:n.1541+83G>T
XM_006721516.3:c.1441G>T	XP_006721579.2:p.Gly481Ter
XM_011523829.2:c.1434+83G>T	XP_011522131.1:n.1434+83G>T
XM_011523830.2:c.1434+83G>T	XP_011522132.1:n.1434+83G>T
XM_024450741.1:c.1434+83G>T	XP_024306509.1:n.1434+83G>T
XR_934021.2:n.1500G>T
XR_934022.2:n.1493+83G>T
XR_934023.2:n.1493+83G>T
NM_000018.4:c.1441G>T MANE Select	NP_000009.1:p.Gly481Ter
NM_001033859.3:c.1375G>T	NP_001029031.1:p.Gly459Ter
NM_001270447.2:c.1510G>T	NP_001257376.1:p.Gly504Ter
NM_001270448.2:c.1213G>T	NP_001257377.1:p.Gly405Ter