Canonical Allele Identifier: CA497620255
Gene: ACADVL HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7126136C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222817C>G , CM000679.2:g.7222817C>G GRCh38
NC_000017.10:g.7126136C>G , CM000679.1:g.7126136C>G GRCh37
NC_000017.9:g.7066860C>G NCBI36
NG_007975.1:g.7984C>G
NG_008391.2:g.2234G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1029C>G MANE Select ENSP00000349297.5:p.Gly343=
ENST00000322910.9:c.*984C>G ENSP00000325395.5:n.*984C>G
ENST00000350303.9:c.963C>G ENSP00000344152.5:p.Gly321=
ENST00000356839.9:c.1029C>G ENSP00000349297.5:p.Gly343=
ENST00000543245.6:c.1098C>G ENSP00000438689.2:p.Gly366=
ENST00000578824.5:n.178C>G
ENST00000581378.5:c.747C>G
ENST00000582379.1:n.413C>G
ENST00000583858.5:c.58C>G
NM_000018.3:c.1029C>G NP_000009.1:p.Gly343=
NM_001033859.2:c.963C>G NP_001029031.1:p.Gly321=
NM_001270447.1:c.1098C>G NP_001257376.1:p.Gly366=
NM_001270448.1:c.801C>G NP_001257377.1:p.Gly267=
XM_006721516.2:c.1029C>G XP_006721579.2:p.Gly343=
XM_011523829.1:c.1029C>G XP_011522131.1:p.Gly343=
XM_011523830.1:c.1029C>G XP_011522132.1:p.Gly343=
XR_934021.1:n.1136C>G
XR_934022.1:n.1136C>G
XR_934023.1:n.1136C>G
XM_006721516.3:c.1029C>G XP_006721579.2:p.Gly343=
XM_011523829.2:c.1029C>G XP_011522131.1:p.Gly343=
XM_011523830.2:c.1029C>G XP_011522132.1:p.Gly343=
XM_024450741.1:c.1029C>G XP_024306509.1:p.Gly343=
XR_934021.2:n.1088C>G
XR_934022.2:n.1088C>G
XR_934023.2:n.1088C>G
NM_000018.4:c.1029C>G MANE Select NP_000009.1:p.Gly343=
NM_001033859.3:c.963C>G NP_001029031.1:p.Gly321=
NM_001270447.2:c.1098C>G NP_001257376.1:p.Gly366=
NM_001270448.2:c.801C>G NP_001257377.1:p.Gly267=
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