Canonical Allele Identifier: CA397723238
Gene: ACADVL HGNC NCBI

Linked Data

dbSNP Id: rs1305511499
MyVariant Identifiers: chr17:g.7124974G>C (hg19) chr17:g.7221655G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221655G>C , CM000679.2:g.7221655G>C GRCh38
NC_000017.10:g.7124974G>C , CM000679.1:g.7124974G>C GRCh37
NC_000017.9:g.7065698G>C NCBI36
NG_007975.1:g.6822G>C
NG_008391.2:g.3396C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.595G>C MANE Select ENSP00000349297.5:p.Glu199Gln
ENST00000322910.9:c.*550G>C ENSP00000325395.5:n.*550G>C
ENST00000350303.9:c.529G>C ENSP00000344152.5:p.Glu177Gln
ENST00000356839.9:c.595G>C ENSP00000349297.5:p.Glu199Gln
ENST00000543245.6:c.664G>C ENSP00000438689.2:p.Glu222Gln
ENST00000577191.5:n.672G>C
ENST00000577433.5:n.803G>C
ENST00000577857.5:n.411G>C
ENST00000579286.5:n.776G>C
ENST00000579886.2:c.433G>C ENSP00000463246.1:p.Glu145Gln
ENST00000580365.1:n.326G>C
ENST00000581378.5:c.313G>C
ENST00000581562.5:n.525-297G>C
ENST00000583312.5:c.595G>C ENSP00000467920.1:p.Glu199Gln
ENST00000583760.1:n.377G>C
NM_000018.3:c.595G>C NP_000009.1:p.Glu199Gln
NM_001033859.2:c.529G>C NP_001029031.1:p.Glu177Gln
NM_001270447.1:c.664G>C NP_001257376.1:p.Glu222Gln
NM_001270448.1:c.367G>C NP_001257377.1:p.Glu123Gln
XM_006721516.2:c.595G>C XP_006721579.2:p.Glu199Gln
XM_011523829.1:c.595G>C XP_011522131.1:p.Glu199Gln
XM_011523830.1:c.595G>C XP_011522132.1:p.Glu199Gln
XR_934021.1:n.702G>C
XR_934022.1:n.702G>C
XR_934023.1:n.702G>C
XM_006721516.3:c.595G>C XP_006721579.2:p.Glu199Gln
XM_011523829.2:c.595G>C XP_011522131.1:p.Glu199Gln
XM_011523830.2:c.595G>C XP_011522132.1:p.Glu199Gln
XM_024450741.1:c.595G>C XP_024306509.1:p.Glu199Gln
XR_934021.2:n.654G>C
XR_934022.2:n.654G>C
XR_934023.2:n.654G>C
NM_000018.4:c.595G>C MANE Select NP_000009.1:p.Glu199Gln
NM_001033859.3:c.529G>C NP_001029031.1:p.Glu177Gln
NM_001270447.2:c.664G>C NP_001257376.1:p.Glu222Gln
NM_001270448.2:c.367G>C NP_001257377.1:p.Glu123Gln
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