Canonical Allele Identifier: CA497694550

Gene: ACADVL

Linked Data

• MyVariant Identifiers: chr17:g.7128317T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7224998T>G , CM000679.2:g.7224998T>G	GRCh38
NC_000017.10:g.7128317T>G , CM000679.1:g.7128317T>G	GRCh37
NC_000017.9:g.7069041T>G	NCBI36
NG_007975.1:g.10165T>G
NG_008391.2:g.53A>C
NG_033038.1:g.14547A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1869T>G MANE Select	ENSP00000349297.5:p.Ser623=
ENST00000322910.9:c.*1824T>G	ENSP00000325395.5:n.*1824T>G
ENST00000350303.9:c.1803T>G	ENSP00000344152.5:p.Ser601=
ENST00000356839.9:c.1869T>G	ENSP00000349297.5:p.Ser623=
ENST00000542255.6:c.748T>G
ENST00000543245.6:c.1938T>G	ENSP00000438689.2:p.Ser646=
ENST00000578033.1:n.294T>G
ENST00000578319.5:n.450T>G
ENST00000578711.1:n.1494T>G
ENST00000578809.5:n.441T>G
ENST00000579425.5:n.985T>G
ENST00000583848.5:c.235T>G	ENSP00000466487.1:n.235T>G
ENST00000583850.5:n.640T>G
ENST00000583858.5:c.800T>G
NM_000018.3:c.1869T>G	NP_000009.1:p.Ser623=
NM_001033859.2:c.1803T>G	NP_001029031.1:p.Ser601=
NM_001270447.1:c.1938T>G	NP_001257376.1:p.Ser646=
NM_001270448.1:c.1641T>G	NP_001257377.1:p.Ser547=
XM_006721516.2:c.1890T>G	XP_006721579.2:p.Ser630=
XM_011523829.1:c.1788T>G	XP_011522131.1:p.Ser596=
XM_011523830.1:c.1767T>G	XP_011522132.1:p.Ser589=
XR_934021.1:n.1972T>G
XR_934022.1:n.1878T>G
XR_934023.1:n.1899T>G
XM_006721516.3:c.1890T>G	XP_006721579.2:p.Ser630=
XM_011523829.2:c.1788T>G	XP_011522131.1:p.Ser596=
XM_011523830.2:c.1767T>G	XP_011522132.1:p.Ser589=
XM_024450741.1:c.1857T>G	XP_024306509.1:p.Ser619=
XR_934021.2:n.1924T>G
XR_934022.2:n.1830T>G
XR_934023.2:n.1851T>G
NM_000018.4:c.1869T>G MANE Select	NP_000009.1:p.Ser623=
NM_001033859.3:c.1803T>G	NP_001029031.1:p.Ser601=
NM_001270447.2:c.1938T>G	NP_001257376.1:p.Ser646=
NM_001270448.2:c.1641T>G	NP_001257377.1:p.Ser547=