Canonical Allele Identifier: CA397724638
Gene: ACADVL HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7127006C>A (hg19) chr17:g.7223687C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7223687C>A , CM000679.2:g.7223687C>A GRCh38
NC_000017.10:g.7127006C>A , CM000679.1:g.7127006C>A GRCh37
NC_000017.9:g.7067730C>A NCBI36
NG_007975.1:g.8854C>A
NG_008391.2:g.1364G>T
NG_033038.1:g.15858G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1226C>A MANE Select ENSP00000349297.5:p.Thr409Lys
ENST00000322910.9:c.*1181C>A ENSP00000325395.5:n.*1181C>A
ENST00000350303.9:c.1160C>A ENSP00000344152.5:p.Thr387Lys
ENST00000356839.9:c.1226C>A ENSP00000349297.5:p.Thr409Lys
ENST00000542255.6:c.84C>A
ENST00000543245.6:c.1295C>A ENSP00000438689.2:p.Thr432Lys
ENST00000578579.2:n.397C>A
ENST00000578711.1:n.183C>A
ENST00000578824.5:n.642C>A
ENST00000579425.5:n.250C>A
ENST00000579546.1:c.63C>A
ENST00000583850.5:n.1C>A
ENST00000583858.5:c.255C>A
ENST00000585203.6:n.434C>A
NM_000018.3:c.1226C>A NP_000009.1:p.Thr409Lys
NM_001033859.2:c.1160C>A NP_001029031.1:p.Thr387Lys
NM_001270447.1:c.1295C>A NP_001257376.1:p.Thr432Lys
NM_001270448.1:c.998C>A NP_001257377.1:p.Thr333Lys
XM_006721516.2:c.1226C>A XP_006721579.2:p.Thr409Lys
XM_011523829.1:c.1226C>A XP_011522131.1:p.Thr409Lys
XM_011523830.1:c.1226C>A XP_011522132.1:p.Thr409Lys
XR_934021.1:n.1333C>A
XR_934022.1:n.1333C>A
XR_934023.1:n.1333C>A
XM_006721516.3:c.1226C>A XP_006721579.2:p.Thr409Lys
XM_011523829.2:c.1226C>A XP_011522131.1:p.Thr409Lys
XM_011523830.2:c.1226C>A XP_011522132.1:p.Thr409Lys
XM_024450741.1:c.1226C>A XP_024306509.1:p.Thr409Lys
XR_934021.2:n.1285C>A
XR_934022.2:n.1285C>A
XR_934023.2:n.1285C>A
NM_000018.4:c.1226C>A MANE Select NP_000009.1:p.Thr409Lys
NM_001033859.3:c.1160C>A NP_001029031.1:p.Thr387Lys
NM_001270447.2:c.1295C>A NP_001257376.1:p.Thr432Lys
NM_001270448.2:c.998C>A NP_001257377.1:p.Thr333Lys
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