Canonical Allele Identifier: CA497694430

Gene: ACADVL

Linked Data

• MyVariant Identifiers: chr17:g.7127972C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7224653C>T , CM000679.2:g.7224653C>T	GRCh38
NC_000017.10:g.7127972C>T , CM000679.1:g.7127972C>T	GRCh37
NC_000017.9:g.7068696C>T	NCBI36
NG_007975.1:g.9820C>T
NG_008391.2:g.398G>A
NG_033038.1:g.14892G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000356839.10:c.1690C>T MANE Select	ENSP00000349297.5:p.Leu564=
ENST00000322910.9:c.*1645C>T	ENSP00000325395.5:n.*1645C>T
ENST00000350303.9:c.1624C>T	ENSP00000344152.5:p.Leu542=
ENST00000356839.9:c.1690C>T	ENSP00000349297.5:p.Leu564=
ENST00000542255.6:c.537-62C>T
ENST00000543245.6:c.1759C>T	ENSP00000438689.2:p.Leu587=
ENST00000578033.1:n.21C>T
ENST00000578319.5:n.271C>T
ENST00000578711.1:n.1149C>T
ENST00000578809.5:n.262C>T
ENST00000579425.5:n.806C>T
ENST00000579546.1:c.425C>T
ENST00000582450.1:n.287C>T
ENST00000583074.5:n.300-62C>T
ENST00000583848.5:c.65-9C>T	ENSP00000466487.1:n.65-9C>T
ENST00000583850.5:n.461C>T
ENST00000583858.5:c.621C>T
ENST00000585203.6:n.881C>T
NM_000018.3:c.1690C>T	NP_000009.1:p.Leu564=
NM_001033859.2:c.1624C>T	NP_001029031.1:p.Leu542=
NM_001270447.1:c.1759C>T	NP_001257376.1:p.Leu587=
NM_001270448.1:c.1462C>T	NP_001257377.1:p.Leu488=
XM_006721516.2:c.1679-62C>T	XP_006721579.2:n.1679-62C>T
XM_011523829.1:c.1577-62C>T	XP_011522131.1:n.1577-62C>T
XM_011523830.1:c.1588C>T	XP_011522132.1:p.Leu530=
XR_934021.1:n.1793C>T
XR_934022.1:n.1699C>T
XR_934023.1:n.1688-62C>T
XM_006721516.3:c.1679-62C>T	XP_006721579.2:n.1679-62C>T
XM_011523829.2:c.1577-62C>T	XP_011522131.1:n.1577-62C>T
XM_011523830.2:c.1588C>T	XP_011522132.1:p.Leu530=
XM_024450741.1:c.1678C>T	XP_024306509.1:p.Leu560=
XR_934021.2:n.1745C>T
XR_934022.2:n.1651C>T
XR_934023.2:n.1640-62C>T
NM_000018.4:c.1690C>T MANE Select	NP_000009.1:p.Leu564=
NM_001033859.3:c.1624C>T	NP_001029031.1:p.Leu542=
NM_001270447.2:c.1759C>T	NP_001257376.1:p.Leu587=
NM_001270448.2:c.1462C>T	NP_001257377.1:p.Leu488=