Canonical Allele Identifier: CA397724489

Gene: ACADVL

Linked Data

• MyVariant Identifiers: chr17:g.7126538G>T (hg19) ; chr17:g.7223219G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7223219G>T , CM000679.2:g.7223219G>T	GRCh38
NC_000017.10:g.7126538G>T , CM000679.1:g.7126538G>T	GRCh37
NC_000017.9:g.7067262G>T	NCBI36
NG_007975.1:g.8386G>T
NG_008391.2:g.1832C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1164G>T MANE Select	ENSP00000349297.5:p.Met388Ile
ENST00000322910.9:c.*1119G>T	ENSP00000325395.5:n.*1119G>T
ENST00000350303.9:c.1098G>T	ENSP00000344152.5:p.Met366Ile
ENST00000356839.9:c.1164G>T	ENSP00000349297.5:p.Met388Ile
ENST00000542255.6:c.22G>T
ENST00000543245.6:c.1233G>T	ENSP00000438689.2:p.Met411Ile
ENST00000578579.2:n.113G>T
ENST00000578824.5:n.580G>T
ENST00000579425.5:n.188G>T
ENST00000579546.1:c.1G>T
ENST00000582379.1:n.815G>T
ENST00000583858.5:c.193G>T
ENST00000585203.6:n.372G>T
NM_000018.3:c.1164G>T	NP_000009.1:p.Met388Ile
NM_001033859.2:c.1098G>T	NP_001029031.1:p.Met366Ile
NM_001270447.1:c.1233G>T	NP_001257376.1:p.Met411Ile
NM_001270448.1:c.936G>T	NP_001257377.1:p.Met312Ile
XM_006721516.2:c.1164G>T	XP_006721579.2:p.Met388Ile
XM_011523829.1:c.1164G>T	XP_011522131.1:p.Met388Ile
XM_011523830.1:c.1164G>T	XP_011522132.1:p.Met388Ile
XR_934021.1:n.1271G>T
XR_934022.1:n.1271G>T
XR_934023.1:n.1271G>T
XM_006721516.3:c.1164G>T	XP_006721579.2:p.Met388Ile
XM_011523829.2:c.1164G>T	XP_011522131.1:p.Met388Ile
XM_011523830.2:c.1164G>T	XP_011522132.1:p.Met388Ile
XM_024450741.1:c.1164G>T	XP_024306509.1:p.Met388Ile
XR_934021.2:n.1223G>T
XR_934022.2:n.1223G>T
XR_934023.2:n.1223G>T
NM_000018.4:c.1164G>T MANE Select	NP_000009.1:p.Met388Ile
NM_001033859.3:c.1098G>T	NP_001029031.1:p.Met366Ile
NM_001270447.2:c.1233G>T	NP_001257376.1:p.Met411Ile
NM_001270448.2:c.936G>T	NP_001257377.1:p.Met312Ile