Canonical Allele Identifier: CA397725044
Gene: ACADVL HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7127357T>C (hg19) chr17:g.7224038T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224038T>C , CM000679.2:g.7224038T>C GRCh38
NC_000017.10:g.7127357T>C , CM000679.1:g.7127357T>C GRCh37
NC_000017.9:g.7068081T>C NCBI36
NG_007975.1:g.9205T>C
NG_008391.2:g.1013A>G
NG_033038.1:g.15507A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1403T>C MANE Select ENSP00000349297.5:p.Leu468Pro
ENST00000322910.9:c.*1358T>C ENSP00000325395.5:n.*1358T>C
ENST00000350303.9:c.1337T>C ENSP00000344152.5:p.Leu446Pro
ENST00000356839.9:c.1403T>C ENSP00000349297.5:p.Leu468Pro
ENST00000542255.6:c.261T>C
ENST00000543245.6:c.1472T>C ENSP00000438689.2:p.Leu491Pro
ENST00000578711.1:n.534T>C
ENST00000579425.5:n.519T>C
ENST00000579546.1:c.240T>C
ENST00000579894.5:n.114T>C
ENST00000583074.5:n.122T>C
ENST00000583850.5:n.178T>C
ENST00000583858.5:c.432T>C
ENST00000585203.6:n.594T>C
NM_000018.3:c.1403T>C NP_000009.1:p.Leu468Pro
NM_001033859.2:c.1337T>C NP_001029031.1:p.Leu446Pro
NM_001270447.1:c.1472T>C NP_001257376.1:p.Leu491Pro
NM_001270448.1:c.1175T>C NP_001257377.1:p.Leu392Pro
XM_006721516.2:c.1403T>C XP_006721579.2:p.Leu468Pro
XM_011523829.1:c.1403T>C XP_011522131.1:p.Leu468Pro
XM_011523830.1:c.1403T>C XP_011522132.1:p.Leu468Pro
XR_934021.1:n.1510T>C
XR_934022.1:n.1510T>C
XR_934023.1:n.1510T>C
XM_006721516.3:c.1403T>C XP_006721579.2:p.Leu468Pro
XM_011523829.2:c.1403T>C XP_011522131.1:p.Leu468Pro
XM_011523830.2:c.1403T>C XP_011522132.1:p.Leu468Pro
XM_024450741.1:c.1403T>C XP_024306509.1:p.Leu468Pro
XR_934021.2:n.1462T>C
XR_934022.2:n.1462T>C
XR_934023.2:n.1462T>C
NM_000018.4:c.1403T>C MANE Select NP_000009.1:p.Leu468Pro
NM_001033859.3:c.1337T>C NP_001029031.1:p.Leu446Pro
NM_001270447.2:c.1472T>C NP_001257376.1:p.Leu491Pro
NM_001270448.2:c.1175T>C NP_001257377.1:p.Leu392Pro
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