Canonical Allele Identifier: CA397723918
Gene: ACADVL HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7126000A>T (hg19) chr17:g.7222681A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222681A>T , CM000679.2:g.7222681A>T GRCh38
NC_000017.10:g.7126000A>T , CM000679.1:g.7126000A>T GRCh37
NC_000017.9:g.7066724A>T NCBI36
NG_007975.1:g.7848A>T
NG_008391.2:g.2370T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.893A>T MANE Select ENSP00000349297.5:p.Lys298Met
ENST00000322910.9:c.*848A>T ENSP00000325395.5:n.*848A>T
ENST00000350303.9:c.827A>T ENSP00000344152.5:p.Lys276Met
ENST00000356839.9:c.893A>T ENSP00000349297.5:p.Lys298Met
ENST00000543245.6:c.962A>T ENSP00000438689.2:p.Lys321Met
ENST00000578824.5:n.42A>T
ENST00000581378.5:c.611A>T
ENST00000582379.1:n.277A>T
NM_000018.3:c.893A>T NP_000009.1:p.Lys298Met
NM_001033859.2:c.827A>T NP_001029031.1:p.Lys276Met
NM_001270447.1:c.962A>T NP_001257376.1:p.Lys321Met
NM_001270448.1:c.665A>T NP_001257377.1:p.Lys222Met
XM_006721516.2:c.893A>T XP_006721579.2:p.Lys298Met
XM_011523829.1:c.893A>T XP_011522131.1:p.Lys298Met
XM_011523830.1:c.893A>T XP_011522132.1:p.Lys298Met
XR_934021.1:n.1000A>T
XR_934022.1:n.1000A>T
XR_934023.1:n.1000A>T
XM_006721516.3:c.893A>T XP_006721579.2:p.Lys298Met
XM_011523829.2:c.893A>T XP_011522131.1:p.Lys298Met
XM_011523830.2:c.893A>T XP_011522132.1:p.Lys298Met
XM_024450741.1:c.893A>T XP_024306509.1:p.Lys298Met
XR_934021.2:n.952A>T
XR_934022.2:n.952A>T
XR_934023.2:n.952A>T
NM_000018.4:c.893A>T MANE Select NP_000009.1:p.Lys298Met
NM_001033859.3:c.827A>T NP_001029031.1:p.Lys276Met
NM_001270447.2:c.962A>T NP_001257376.1:p.Lys321Met
NM_001270448.2:c.665A>T NP_001257377.1:p.Lys222Met
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