Canonical Allele Identifier: CA397723666
Gene: ACADVL HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7125519T>A (hg19) chr17:g.7222200T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222200T>A , CM000679.2:g.7222200T>A GRCh38
NC_000017.10:g.7125519T>A , CM000679.1:g.7125519T>A GRCh37
NC_000017.9:g.7066243T>A NCBI36
NG_007975.1:g.7367T>A
NG_008391.2:g.2851A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.776T>A MANE Select ENSP00000349297.5:p.Phe259Tyr
ENST00000322910.9:c.*731T>A ENSP00000325395.5:n.*731T>A
ENST00000350303.9:c.710T>A ENSP00000344152.5:p.Phe237Tyr
ENST00000356839.9:c.776T>A ENSP00000349297.5:p.Phe259Tyr
ENST00000543245.6:c.845T>A ENSP00000438689.2:p.Phe282Tyr
ENST00000577191.5:n.948T>A
ENST00000581378.5:c.494T>A
ENST00000582379.1:n.160T>A
NM_000018.3:c.776T>A NP_000009.1:p.Phe259Tyr
NM_001033859.2:c.710T>A NP_001029031.1:p.Phe237Tyr
NM_001270447.1:c.845T>A NP_001257376.1:p.Phe282Tyr
NM_001270448.1:c.548T>A NP_001257377.1:p.Phe183Tyr
XM_006721516.2:c.776T>A XP_006721579.2:p.Phe259Tyr
XM_011523829.1:c.776T>A XP_011522131.1:p.Phe259Tyr
XM_011523830.1:c.776T>A XP_011522132.1:p.Phe259Tyr
XR_934021.1:n.883T>A
XR_934022.1:n.883T>A
XR_934023.1:n.883T>A
XM_006721516.3:c.776T>A XP_006721579.2:p.Phe259Tyr
XM_011523829.2:c.776T>A XP_011522131.1:p.Phe259Tyr
XM_011523830.2:c.776T>A XP_011522132.1:p.Phe259Tyr
XM_024450741.1:c.776T>A XP_024306509.1:p.Phe259Tyr
XR_934021.2:n.835T>A
XR_934022.2:n.835T>A
XR_934023.2:n.835T>A
NM_000018.4:c.776T>A MANE Select NP_000009.1:p.Phe259Tyr
NM_001033859.3:c.710T>A NP_001029031.1:p.Phe237Tyr
NM_001270447.2:c.845T>A NP_001257376.1:p.Phe282Tyr
NM_001270448.2:c.548T>A NP_001257377.1:p.Phe183Tyr
Search 100 bp 5'
Search 100 bp 3'