Canonical Allele Identifier: CA397724987

Gene: ACADVL

Linked Data

• MyVariant Identifiers: chr17:g.7127332A>T (hg19) ; chr17:g.7224013A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7224013A>T , CM000679.2:g.7224013A>T	GRCh38
NC_000017.10:g.7127332A>T , CM000679.1:g.7127332A>T	GRCh37
NC_000017.9:g.7068056A>T	NCBI36
NG_007975.1:g.9180A>T
NG_008391.2:g.1038T>A
NG_033038.1:g.15532T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000356839.10:c.1378A>T MANE Select	ENSP00000349297.5:p.Ile460Phe
ENST00000322910.9:c.*1333A>T	ENSP00000325395.5:n.*1333A>T
ENST00000350303.9:c.1312A>T	ENSP00000344152.5:p.Ile438Phe
ENST00000356839.9:c.1378A>T	ENSP00000349297.5:p.Ile460Phe
ENST00000542255.6:c.236A>T
ENST00000543245.6:c.1447A>T	ENSP00000438689.2:p.Ile483Phe
ENST00000578711.1:n.509A>T
ENST00000579425.5:n.494A>T
ENST00000579546.1:c.215A>T
ENST00000579894.5:n.89A>T
ENST00000583074.5:n.97A>T
ENST00000583850.5:n.153A>T
ENST00000583858.5:c.407A>T
ENST00000585203.6:n.569A>T
NM_000018.3:c.1378A>T	NP_000009.1:p.Ile460Phe
NM_001033859.2:c.1312A>T	NP_001029031.1:p.Ile438Phe
NM_001270447.1:c.1447A>T	NP_001257376.1:p.Ile483Phe
NM_001270448.1:c.1150A>T	NP_001257377.1:p.Ile384Phe
XM_006721516.2:c.1378A>T	XP_006721579.2:p.Ile460Phe
XM_011523829.1:c.1378A>T	XP_011522131.1:p.Ile460Phe
XM_011523830.1:c.1378A>T	XP_011522132.1:p.Ile460Phe
XR_934021.1:n.1485A>T
XR_934022.1:n.1485A>T
XR_934023.1:n.1485A>T
XM_006721516.3:c.1378A>T	XP_006721579.2:p.Ile460Phe
XM_011523829.2:c.1378A>T	XP_011522131.1:p.Ile460Phe
XM_011523830.2:c.1378A>T	XP_011522132.1:p.Ile460Phe
XM_024450741.1:c.1378A>T	XP_024306509.1:p.Ile460Phe
XR_934021.2:n.1437A>T
XR_934022.2:n.1437A>T
XR_934023.2:n.1437A>T
NM_000018.4:c.1378A>T MANE Select	NP_000009.1:p.Ile460Phe
NM_001033859.3:c.1312A>T	NP_001029031.1:p.Ile438Phe
NM_001270447.2:c.1447A>T	NP_001257376.1:p.Ile483Phe
NM_001270448.2:c.1150A>T	NP_001257377.1:p.Ile384Phe