Canonical Allele Identifier: CA497694015

Gene: ACADVL

Linked Data

• MyVariant Identifiers: chr17:g.7125326C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7222007C>G , CM000679.2:g.7222007C>G	GRCh38
NC_000017.10:g.7125326C>G , CM000679.1:g.7125326C>G	GRCh37
NC_000017.9:g.7066050C>G	NCBI36
NG_007975.1:g.7174C>G
NG_008391.2:g.3044G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000356839.10:c.678C>G MANE Select	ENSP00000349297.5:p.Ala226=
ENST00000322910.9:c.*633C>G	ENSP00000325395.5:n.*633C>G
ENST00000350303.9:c.612C>G	ENSP00000344152.5:p.Ala204=
ENST00000356839.9:c.678C>G	ENSP00000349297.5:p.Ala226=
ENST00000543245.6:c.747C>G	ENSP00000438689.2:p.Ala249=
ENST00000577191.5:n.755C>G
ENST00000577857.5:n.494C>G
ENST00000579286.5:n.859C>G
ENST00000580365.1:n.409C>G
ENST00000581378.5:c.396C>G
ENST00000582379.1:n.62C>G
ENST00000583760.1:n.460C>G
NM_000018.3:c.678C>G	NP_000009.1:p.Ala226=
NM_001033859.2:c.612C>G	NP_001029031.1:p.Ala204=
NM_001270447.1:c.747C>G	NP_001257376.1:p.Ala249=
NM_001270448.1:c.450C>G	NP_001257377.1:p.Ala150=
XM_006721516.2:c.678C>G	XP_006721579.2:p.Ala226=
XM_011523829.1:c.678C>G	XP_011522131.1:p.Ala226=
XM_011523830.1:c.678C>G	XP_011522132.1:p.Ala226=
XR_934021.1:n.785C>G
XR_934022.1:n.785C>G
XR_934023.1:n.785C>G
XM_006721516.3:c.678C>G	XP_006721579.2:p.Ala226=
XM_011523829.2:c.678C>G	XP_011522131.1:p.Ala226=
XM_011523830.2:c.678C>G	XP_011522132.1:p.Ala226=
XM_024450741.1:c.678C>G	XP_024306509.1:p.Ala226=
XR_934021.2:n.737C>G
XR_934022.2:n.737C>G
XR_934023.2:n.737C>G
NM_000018.4:c.678C>G MANE Select	NP_000009.1:p.Ala226=
NM_001033859.3:c.612C>G	NP_001029031.1:p.Ala204=
NM_001270447.2:c.747C>G	NP_001257376.1:p.Ala249=
NM_001270448.2:c.450C>G	NP_001257377.1:p.Ala150=