Canonical Allele Identifier: CA397724273
Gene: ACADVL HGNC NCBI

Linked Data

ClinVar Variation Id: 932875
ClinVar RCV Id: RCV001200839
dbSNP Id: rs1351976589
MyVariant Identifiers: chr17:g.7126171T>G (hg19) chr17:g.7222852T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222852T>G , CM000679.2:g.7222852T>G GRCh38
NC_000017.10:g.7126171T>G , CM000679.1:g.7126171T>G GRCh37
NC_000017.9:g.7066895T>G NCBI36
NG_007975.1:g.8019T>G
NG_008391.2:g.2199A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1064T>G MANE Select ENSP00000349297.5:p.Ile355Ser
ENST00000322910.9:c.*1019T>G ENSP00000325395.5:n.*1019T>G
ENST00000350303.9:c.998T>G ENSP00000344152.5:p.Ile333Ser
ENST00000356839.9:c.1064T>G ENSP00000349297.5:p.Ile355Ser
ENST00000543245.6:c.1133T>G ENSP00000438689.2:p.Ile378Ser
ENST00000578824.5:n.213T>G
ENST00000582379.1:n.448T>G
ENST00000583858.5:c.93T>G
ENST00000585203.6:n.5T>G
NM_000018.3:c.1064T>G NP_000009.1:p.Ile355Ser
NM_001033859.2:c.998T>G NP_001029031.1:p.Ile333Ser
NM_001270447.1:c.1133T>G NP_001257376.1:p.Ile378Ser
NM_001270448.1:c.836T>G NP_001257377.1:p.Ile279Ser
XM_006721516.2:c.1064T>G XP_006721579.2:p.Ile355Ser
XM_011523829.1:c.1064T>G XP_011522131.1:p.Ile355Ser
XM_011523830.1:c.1064T>G XP_011522132.1:p.Ile355Ser
XR_934021.1:n.1171T>G
XR_934022.1:n.1171T>G
XR_934023.1:n.1171T>G
XM_006721516.3:c.1064T>G XP_006721579.2:p.Ile355Ser
XM_011523829.2:c.1064T>G XP_011522131.1:p.Ile355Ser
XM_011523830.2:c.1064T>G XP_011522132.1:p.Ile355Ser
XM_024450741.1:c.1064T>G XP_024306509.1:p.Ile355Ser
XR_934021.2:n.1123T>G
XR_934022.2:n.1123T>G
XR_934023.2:n.1123T>G
NM_000018.4:c.1064T>G MANE Select NP_000009.1:p.Ile355Ser
NM_001033859.3:c.998T>G NP_001029031.1:p.Ile333Ser
NM_001270447.2:c.1133T>G NP_001257376.1:p.Ile378Ser
NM_001270448.2:c.836T>G NP_001257377.1:p.Ile279Ser
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