Canonical Allele Identifier: CA397723692
Gene: ACADVL HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7125531C>T (hg19) chr17:g.7222212C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222212C>T , CM000679.2:g.7222212C>T GRCh38
NC_000017.10:g.7125531C>T , CM000679.1:g.7125531C>T GRCh37
NC_000017.9:g.7066255C>T NCBI36
NG_007975.1:g.7379C>T
NG_008391.2:g.2839G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.788C>T MANE Select ENSP00000349297.5:p.Ala263Val
ENST00000322910.9:c.*743C>T ENSP00000325395.5:n.*743C>T
ENST00000350303.9:c.722C>T ENSP00000344152.5:p.Ala241Val
ENST00000356839.9:c.788C>T ENSP00000349297.5:p.Ala263Val
ENST00000543245.6:c.857C>T ENSP00000438689.2:p.Ala286Val
ENST00000577191.5:n.960C>T
ENST00000581378.5:c.506C>T
ENST00000582379.1:n.172C>T
NM_000018.3:c.788C>T NP_000009.1:p.Ala263Val
NM_001033859.2:c.722C>T NP_001029031.1:p.Ala241Val
NM_001270447.1:c.857C>T NP_001257376.1:p.Ala286Val
NM_001270448.1:c.560C>T NP_001257377.1:p.Ala187Val
XM_006721516.2:c.788C>T XP_006721579.2:p.Ala263Val
XM_011523829.1:c.788C>T XP_011522131.1:p.Ala263Val
XM_011523830.1:c.788C>T XP_011522132.1:p.Ala263Val
XR_934021.1:n.895C>T
XR_934022.1:n.895C>T
XR_934023.1:n.895C>T
XM_006721516.3:c.788C>T XP_006721579.2:p.Ala263Val
XM_011523829.2:c.788C>T XP_011522131.1:p.Ala263Val
XM_011523830.2:c.788C>T XP_011522132.1:p.Ala263Val
XM_024450741.1:c.788C>T XP_024306509.1:p.Ala263Val
XR_934021.2:n.847C>T
XR_934022.2:n.847C>T
XR_934023.2:n.847C>T
NM_000018.4:c.788C>T MANE Select NP_000009.1:p.Ala263Val
NM_001033859.3:c.722C>T NP_001029031.1:p.Ala241Val
NM_001270447.2:c.857C>T NP_001257376.1:p.Ala286Val
NM_001270448.2:c.560C>T NP_001257377.1:p.Ala187Val
Search 100 bp 5'
Search 100 bp 3'