Canonical Allele Identifier: CA397723946
Gene: ACADVL HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7126014A>C (hg19) chr17:g.7222695A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222695A>C , CM000679.2:g.7222695A>C GRCh38
NC_000017.10:g.7126014A>C , CM000679.1:g.7126014A>C GRCh37
NC_000017.9:g.7066738A>C NCBI36
NG_007975.1:g.7862A>C
NG_008391.2:g.2356T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.907A>C MANE Select ENSP00000349297.5:p.Lys303Gln
ENST00000322910.9:c.*862A>C ENSP00000325395.5:n.*862A>C
ENST00000350303.9:c.841A>C ENSP00000344152.5:p.Lys281Gln
ENST00000356839.9:c.907A>C ENSP00000349297.5:p.Lys303Gln
ENST00000543245.6:c.976A>C ENSP00000438689.2:p.Lys326Gln
ENST00000578824.5:n.56A>C
ENST00000581378.5:c.625A>C
ENST00000582379.1:n.291A>C
NM_000018.3:c.907A>C NP_000009.1:p.Lys303Gln
NM_001033859.2:c.841A>C NP_001029031.1:p.Lys281Gln
NM_001270447.1:c.976A>C NP_001257376.1:p.Lys326Gln
NM_001270448.1:c.679A>C NP_001257377.1:p.Lys227Gln
XM_006721516.2:c.907A>C XP_006721579.2:p.Lys303Gln
XM_011523829.1:c.907A>C XP_011522131.1:p.Lys303Gln
XM_011523830.1:c.907A>C XP_011522132.1:p.Lys303Gln
XR_934021.1:n.1014A>C
XR_934022.1:n.1014A>C
XR_934023.1:n.1014A>C
XM_006721516.3:c.907A>C XP_006721579.2:p.Lys303Gln
XM_011523829.2:c.907A>C XP_011522131.1:p.Lys303Gln
XM_011523830.2:c.907A>C XP_011522132.1:p.Lys303Gln
XM_024450741.1:c.907A>C XP_024306509.1:p.Lys303Gln
XR_934021.2:n.966A>C
XR_934022.2:n.966A>C
XR_934023.2:n.966A>C
NM_000018.4:c.907A>C MANE Select NP_000009.1:p.Lys303Gln
NM_001033859.3:c.841A>C NP_001029031.1:p.Lys281Gln
NM_001270447.2:c.976A>C NP_001257376.1:p.Lys326Gln
NM_001270448.2:c.679A>C NP_001257377.1:p.Lys227Gln
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