Canonical Allele Identifier: CA397723056

Gene: ACADVL

Linked Data

• MyVariant Identifiers: chr17:g.7124886G>T (hg19) ; chr17:g.7221567G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7221567G>T , CM000679.2:g.7221567G>T	GRCh38
NC_000017.10:g.7124886G>T , CM000679.1:g.7124886G>T	GRCh37
NC_000017.9:g.7065610G>T	NCBI36
NG_007975.1:g.6734G>T
NG_008391.2:g.3484C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.507G>T MANE Select	ENSP00000349297.5:p.Met169Ile
ENST00000322910.9:c.*462G>T	ENSP00000325395.5:n.*462G>T
ENST00000350303.9:c.441G>T	ENSP00000344152.5:p.Met147Ile
ENST00000356839.9:c.507G>T	ENSP00000349297.5:p.Met169Ile
ENST00000543245.6:c.576G>T	ENSP00000438689.2:p.Met192Ile
ENST00000577191.5:n.584G>T
ENST00000577433.5:n.715G>T
ENST00000577857.5:n.323G>T
ENST00000579286.5:n.688G>T
ENST00000579886.2:c.345G>T	ENSP00000463246.1:p.Met115Ile
ENST00000580365.1:n.238G>T
ENST00000581378.5:c.225G>T
ENST00000581562.5:n.525-385G>T
ENST00000582166.1:n.488G>T
ENST00000583312.5:c.507G>T	ENSP00000467920.1:p.Met169Ile
ENST00000583760.1:n.289G>T
NM_000018.3:c.507G>T	NP_000009.1:p.Met169Ile
NM_001033859.2:c.441G>T	NP_001029031.1:p.Met147Ile
NM_001270447.1:c.576G>T	NP_001257376.1:p.Met192Ile
NM_001270448.1:c.279G>T	NP_001257377.1:p.Met93Ile
XM_006721516.2:c.507G>T	XP_006721579.2:p.Met169Ile
XM_011523829.1:c.507G>T	XP_011522131.1:p.Met169Ile
XM_011523830.1:c.507G>T	XP_011522132.1:p.Met169Ile
XR_934021.1:n.614G>T
XR_934022.1:n.614G>T
XR_934023.1:n.614G>T
XM_006721516.3:c.507G>T	XP_006721579.2:p.Met169Ile
XM_011523829.2:c.507G>T	XP_011522131.1:p.Met169Ile
XM_011523830.2:c.507G>T	XP_011522132.1:p.Met169Ile
XM_024450741.1:c.507G>T	XP_024306509.1:p.Met169Ile
XR_934021.2:n.566G>T
XR_934022.2:n.566G>T
XR_934023.2:n.566G>T
NM_000018.4:c.507G>T MANE Select	NP_000009.1:p.Met169Ile
NM_001033859.3:c.441G>T	NP_001029031.1:p.Met147Ile
NM_001270447.2:c.576G>T	NP_001257376.1:p.Met192Ile
NM_001270448.2:c.279G>T	NP_001257377.1:p.Met93Ile