Canonical Allele Identifier: CA497694029
Gene: ACADVL HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7125344T>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222025T>G , CM000679.2:g.7222025T>G GRCh38
NC_000017.10:g.7125344T>G , CM000679.1:g.7125344T>G GRCh37
NC_000017.9:g.7066068T>G NCBI36
NG_007975.1:g.7192T>G
NG_008391.2:g.3026A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.696T>G MANE Select ENSP00000349297.5:p.Ala232=
ENST00000322910.9:c.*651T>G ENSP00000325395.5:n.*651T>G
ENST00000350303.9:c.630T>G ENSP00000344152.5:p.Ala210=
ENST00000356839.9:c.696T>G ENSP00000349297.5:p.Ala232=
ENST00000543245.6:c.765T>G ENSP00000438689.2:p.Ala255=
ENST00000577191.5:n.773T>G
ENST00000577857.5:n.512T>G
ENST00000579286.5:n.877T>G
ENST00000580365.1:n.427T>G
ENST00000581378.5:c.414T>G
ENST00000582379.1:n.80T>G
ENST00000583760.1:n.478T>G
NM_000018.3:c.696T>G NP_000009.1:p.Ala232=
NM_001033859.2:c.630T>G NP_001029031.1:p.Ala210=
NM_001270447.1:c.765T>G NP_001257376.1:p.Ala255=
NM_001270448.1:c.468T>G NP_001257377.1:p.Ala156=
XM_006721516.2:c.696T>G XP_006721579.2:p.Ala232=
XM_011523829.1:c.696T>G XP_011522131.1:p.Ala232=
XM_011523830.1:c.696T>G XP_011522132.1:p.Ala232=
XR_934021.1:n.803T>G
XR_934022.1:n.803T>G
XR_934023.1:n.803T>G
XM_006721516.3:c.696T>G XP_006721579.2:p.Ala232=
XM_011523829.2:c.696T>G XP_011522131.1:p.Ala232=
XM_011523830.2:c.696T>G XP_011522132.1:p.Ala232=
XM_024450741.1:c.696T>G XP_024306509.1:p.Ala232=
XR_934021.2:n.755T>G
XR_934022.2:n.755T>G
XR_934023.2:n.755T>G
NM_000018.4:c.696T>G MANE Select NP_000009.1:p.Ala232=
NM_001033859.3:c.630T>G NP_001029031.1:p.Ala210=
NM_001270447.2:c.765T>G NP_001257376.1:p.Ala255=
NM_001270448.2:c.468T>G NP_001257377.1:p.Ala156=
Search 100 bp 5'
Search 100 bp 3'