Canonical Allele Identifier: CA397723229
Gene: ACADVL HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7124970G>T (hg19) chr17:g.7221651G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221651G>T , CM000679.2:g.7221651G>T GRCh38
NC_000017.10:g.7124970G>T , CM000679.1:g.7124970G>T GRCh37
NC_000017.9:g.7065694G>T NCBI36
NG_007975.1:g.6818G>T
NG_008391.2:g.3400C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.591G>T MANE Select ENSP00000349297.5:p.Gln197His
ENST00000322910.9:c.*546G>T ENSP00000325395.5:n.*546G>T
ENST00000350303.9:c.525G>T ENSP00000344152.5:p.Gln175His
ENST00000356839.9:c.591G>T ENSP00000349297.5:p.Gln197His
ENST00000543245.6:c.660G>T ENSP00000438689.2:p.Gln220His
ENST00000577191.5:n.668G>T
ENST00000577433.5:n.799G>T
ENST00000577857.5:n.407G>T
ENST00000579286.5:n.772G>T
ENST00000579886.2:c.429G>T ENSP00000463246.1:p.Gln143His
ENST00000580365.1:n.322G>T
ENST00000581378.5:c.309G>T
ENST00000581562.5:n.525-301G>T
ENST00000583312.5:c.591G>T ENSP00000467920.1:p.Gln197His
ENST00000583760.1:n.373G>T
NM_000018.3:c.591G>T NP_000009.1:p.Gln197His
NM_001033859.2:c.525G>T NP_001029031.1:p.Gln175His
NM_001270447.1:c.660G>T NP_001257376.1:p.Gln220His
NM_001270448.1:c.363G>T NP_001257377.1:p.Gln121His
XM_006721516.2:c.591G>T XP_006721579.2:p.Gln197His
XM_011523829.1:c.591G>T XP_011522131.1:p.Gln197His
XM_011523830.1:c.591G>T XP_011522132.1:p.Gln197His
XR_934021.1:n.698G>T
XR_934022.1:n.698G>T
XR_934023.1:n.698G>T
XM_006721516.3:c.591G>T XP_006721579.2:p.Gln197His
XM_011523829.2:c.591G>T XP_011522131.1:p.Gln197His
XM_011523830.2:c.591G>T XP_011522132.1:p.Gln197His
XM_024450741.1:c.591G>T XP_024306509.1:p.Gln197His
XR_934021.2:n.650G>T
XR_934022.2:n.650G>T
XR_934023.2:n.650G>T
NM_000018.4:c.591G>T MANE Select NP_000009.1:p.Gln197His
NM_001033859.3:c.525G>T NP_001029031.1:p.Gln175His
NM_001270447.2:c.660G>T NP_001257376.1:p.Gln220His
NM_001270448.2:c.363G>T NP_001257377.1:p.Gln121His
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