Canonical Allele Identifier: CA397723992
Gene: ACADVL HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7126036T>G (hg19) chr17:g.7222717T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222717T>G , CM000679.2:g.7222717T>G GRCh38
NC_000017.10:g.7126036T>G , CM000679.1:g.7126036T>G GRCh37
NC_000017.9:g.7066760T>G NCBI36
NG_007975.1:g.7884T>G
NG_008391.2:g.2334A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.929T>G MANE Select ENSP00000349297.5:p.Val310Gly
ENST00000322910.9:c.*884T>G ENSP00000325395.5:n.*884T>G
ENST00000350303.9:c.863T>G ENSP00000344152.5:p.Val288Gly
ENST00000356839.9:c.929T>G ENSP00000349297.5:p.Val310Gly
ENST00000543245.6:c.998T>G ENSP00000438689.2:p.Val333Gly
ENST00000578824.5:n.78T>G
ENST00000581378.5:c.647T>G
ENST00000582379.1:n.313T>G
NM_000018.3:c.929T>G NP_000009.1:p.Val310Gly
NM_001033859.2:c.863T>G NP_001029031.1:p.Val288Gly
NM_001270447.1:c.998T>G NP_001257376.1:p.Val333Gly
NM_001270448.1:c.701T>G NP_001257377.1:p.Val234Gly
XM_006721516.2:c.929T>G XP_006721579.2:p.Val310Gly
XM_011523829.1:c.929T>G XP_011522131.1:p.Val310Gly
XM_011523830.1:c.929T>G XP_011522132.1:p.Val310Gly
XR_934021.1:n.1036T>G
XR_934022.1:n.1036T>G
XR_934023.1:n.1036T>G
XM_006721516.3:c.929T>G XP_006721579.2:p.Val310Gly
XM_011523829.2:c.929T>G XP_011522131.1:p.Val310Gly
XM_011523830.2:c.929T>G XP_011522132.1:p.Val310Gly
XM_024450741.1:c.929T>G XP_024306509.1:p.Val310Gly
XR_934021.2:n.988T>G
XR_934022.2:n.988T>G
XR_934023.2:n.988T>G
NM_000018.4:c.929T>G MANE Select NP_000009.1:p.Val310Gly
NM_001033859.3:c.863T>G NP_001029031.1:p.Val288Gly
NM_001270447.2:c.998T>G NP_001257376.1:p.Val333Gly
NM_001270448.2:c.701T>G NP_001257377.1:p.Val234Gly
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