Canonical Allele Identifier: CA497693933

Gene: ACADVL

Linked Data

• MyVariant Identifiers: chr17:g.7123985A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7220666A>T , CM000679.2:g.7220666A>T	GRCh38
NC_000017.10:g.7123985A>T , CM000679.1:g.7123985A>T	GRCh37
NC_000017.9:g.7064709A>T	NCBI36
NG_007975.1:g.5833A>T
NG_008391.2:g.4385T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.267A>T MANE Select	ENSP00000349297.5:p.Pro89=
ENST00000322910.9:c.*222A>T	ENSP00000325395.5:n.*222A>T
ENST00000350303.9:c.201A>T	ENSP00000344152.5:p.Pro67=
ENST00000356839.9:c.267A>T	ENSP00000349297.5:p.Pro89=
ENST00000543245.6:c.336A>T	ENSP00000438689.2:p.Pro112=
ENST00000577191.5:n.344A>T
ENST00000577433.5:n.475A>T
ENST00000577857.5:n.229-100A>T
ENST00000578269.5:n.714A>T
ENST00000578421.1:n.475A>T
ENST00000579286.5:n.448A>T
ENST00000579886.2:c.201+140A>T	ENSP00000463246.1:n.201+140A>T
ENST00000580263.5:n.431A>T
ENST00000581562.5:n.314A>T
ENST00000582056.5:n.357A>T
ENST00000582166.1:n.155A>T
ENST00000582356.5:n.466A>T
ENST00000583312.5:c.267A>T	ENSP00000467920.1:p.Pro89=
ENST00000584103.5:c.267A>T	ENSP00000465353.1:p.Pro89=
NM_000018.3:c.267A>T	NP_000009.1:p.Pro89=
NM_001033859.2:c.201A>T	NP_001029031.1:p.Pro67=
NM_001270447.1:c.336A>T	NP_001257376.1:p.Pro112=
NM_001270448.1:c.39A>T	NP_001257377.1:p.Pro13=
XM_006721516.2:c.267A>T	XP_006721579.2:p.Pro89=
XM_011523829.1:c.267A>T	XP_011522131.1:p.Pro89=
XM_011523830.1:c.267A>T	XP_011522132.1:p.Pro89=
XR_934021.1:n.374A>T
XR_934022.1:n.374A>T
XR_934023.1:n.374A>T
XM_006721516.3:c.267A>T	XP_006721579.2:p.Pro89=
XM_011523829.2:c.267A>T	XP_011522131.1:p.Pro89=
XM_011523830.2:c.267A>T	XP_011522132.1:p.Pro89=
XM_024450741.1:c.267A>T	XP_024306509.1:p.Pro89=
XR_934021.2:n.326A>T
XR_934022.2:n.326A>T
XR_934023.2:n.326A>T
NM_000018.4:c.267A>T MANE Select	NP_000009.1:p.Pro89=
NM_001033859.3:c.201A>T	NP_001029031.1:p.Pro67=
NM_001270447.2:c.336A>T	NP_001257376.1:p.Pro112=
NM_001270448.2:c.39A>T	NP_001257377.1:p.Pro13=