Canonical Allele Identifier: CA397724676
Gene: ACADVL HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7127023G>T (hg19) chr17:g.7223704G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7223704G>T , CM000679.2:g.7223704G>T GRCh38
NC_000017.10:g.7127023G>T , CM000679.1:g.7127023G>T GRCh37
NC_000017.9:g.7067747G>T NCBI36
NG_007975.1:g.8871G>T
NG_008391.2:g.1347C>A
NG_033038.1:g.15841C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1243G>T MANE Select ENSP00000349297.5:p.Ala415Ser
ENST00000322910.9:c.*1198G>T ENSP00000325395.5:n.*1198G>T
ENST00000350303.9:c.1177G>T ENSP00000344152.5:p.Ala393Ser
ENST00000356839.9:c.1243G>T ENSP00000349297.5:p.Ala415Ser
ENST00000542255.6:c.101G>T
ENST00000543245.6:c.1312G>T ENSP00000438689.2:p.Ala438Ser
ENST00000578579.2:n.414G>T
ENST00000578711.1:n.200G>T
ENST00000578824.5:n.659G>T
ENST00000579425.5:n.267G>T
ENST00000579546.1:c.80G>T
ENST00000583850.5:n.18G>T
ENST00000583858.5:c.272G>T
ENST00000585203.6:n.451G>T
NM_000018.3:c.1243G>T NP_000009.1:p.Ala415Ser
NM_001033859.2:c.1177G>T NP_001029031.1:p.Ala393Ser
NM_001270447.1:c.1312G>T NP_001257376.1:p.Ala438Ser
NM_001270448.1:c.1015G>T NP_001257377.1:p.Ala339Ser
XM_006721516.2:c.1243G>T XP_006721579.2:p.Ala415Ser
XM_011523829.1:c.1243G>T XP_011522131.1:p.Ala415Ser
XM_011523830.1:c.1243G>T XP_011522132.1:p.Ala415Ser
XR_934021.1:n.1350G>T
XR_934022.1:n.1350G>T
XR_934023.1:n.1350G>T
XM_006721516.3:c.1243G>T XP_006721579.2:p.Ala415Ser
XM_011523829.2:c.1243G>T XP_011522131.1:p.Ala415Ser
XM_011523830.2:c.1243G>T XP_011522132.1:p.Ala415Ser
XM_024450741.1:c.1243G>T XP_024306509.1:p.Ala415Ser
XR_934021.2:n.1302G>T
XR_934022.2:n.1302G>T
XR_934023.2:n.1302G>T
NM_000018.4:c.1243G>T MANE Select NP_000009.1:p.Ala415Ser
NM_001033859.3:c.1177G>T NP_001029031.1:p.Ala393Ser
NM_001270447.2:c.1312G>T NP_001257376.1:p.Ala438Ser
NM_001270448.2:c.1015G>T NP_001257377.1:p.Ala339Ser
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