Canonical Allele Identifier: CA497620176
Gene: ACADVL HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7126010C>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222691C>G , CM000679.2:g.7222691C>G GRCh38
NC_000017.10:g.7126010C>G , CM000679.1:g.7126010C>G GRCh37
NC_000017.9:g.7066734C>G NCBI36
NG_007975.1:g.7858C>G
NG_008391.2:g.2360G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.903C>G MANE Select ENSP00000349297.5:p.Gly301=
ENST00000322910.9:c.*858C>G ENSP00000325395.5:n.*858C>G
ENST00000350303.9:c.837C>G ENSP00000344152.5:p.Gly279=
ENST00000356839.9:c.903C>G ENSP00000349297.5:p.Gly301=
ENST00000543245.6:c.972C>G ENSP00000438689.2:p.Gly324=
ENST00000578824.5:n.52C>G
ENST00000581378.5:c.621C>G
ENST00000582379.1:n.287C>G
NM_000018.3:c.903C>G NP_000009.1:p.Gly301=
NM_001033859.2:c.837C>G NP_001029031.1:p.Gly279=
NM_001270447.1:c.972C>G NP_001257376.1:p.Gly324=
NM_001270448.1:c.675C>G NP_001257377.1:p.Gly225=
XM_006721516.2:c.903C>G XP_006721579.2:p.Gly301=
XM_011523829.1:c.903C>G XP_011522131.1:p.Gly301=
XM_011523830.1:c.903C>G XP_011522132.1:p.Gly301=
XR_934021.1:n.1010C>G
XR_934022.1:n.1010C>G
XR_934023.1:n.1010C>G
XM_006721516.3:c.903C>G XP_006721579.2:p.Gly301=
XM_011523829.2:c.903C>G XP_011522131.1:p.Gly301=
XM_011523830.2:c.903C>G XP_011522132.1:p.Gly301=
XM_024450741.1:c.903C>G XP_024306509.1:p.Gly301=
XR_934021.2:n.962C>G
XR_934022.2:n.962C>G
XR_934023.2:n.962C>G
NM_000018.4:c.903C>G MANE Select NP_000009.1:p.Gly301=
NM_001033859.3:c.837C>G NP_001029031.1:p.Gly279=
NM_001270447.2:c.972C>G NP_001257376.1:p.Gly324=
NM_001270448.2:c.675C>G NP_001257377.1:p.Gly225=
Search 100 bp 5'
Search 100 bp 3'