Canonical Allele Identifier: CA497693802
Gene: ACADVL HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7124979A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221660A>G , CM000679.2:g.7221660A>G GRCh38
NC_000017.10:g.7124979A>G , CM000679.1:g.7124979A>G GRCh37
NC_000017.9:g.7065703A>G NCBI36
NG_007975.1:g.6827A>G
NG_008391.2:g.3391T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.600A>G MANE Select ENSP00000349297.5:p.Lys200=
ENST00000322910.9:c.*555A>G ENSP00000325395.5:n.*555A>G
ENST00000350303.9:c.534A>G ENSP00000344152.5:p.Lys178=
ENST00000356839.9:c.600A>G ENSP00000349297.5:p.Lys200=
ENST00000543245.6:c.669A>G ENSP00000438689.2:p.Lys223=
ENST00000577191.5:n.677A>G
ENST00000577857.5:n.416A>G
ENST00000579286.5:n.781A>G
ENST00000579886.2:c.438A>G ENSP00000463246.1:p.Lys146=
ENST00000580365.1:n.331A>G
ENST00000581378.5:c.318A>G
ENST00000581562.5:n.525-292A>G
ENST00000583312.5:c.600A>G ENSP00000467920.1:p.Lys200=
ENST00000583760.1:n.382A>G
NM_000018.3:c.600A>G NP_000009.1:p.Lys200=
NM_001033859.2:c.534A>G NP_001029031.1:p.Lys178=
NM_001270447.1:c.669A>G NP_001257376.1:p.Lys223=
NM_001270448.1:c.372A>G NP_001257377.1:p.Lys124=
XM_006721516.2:c.600A>G XP_006721579.2:p.Lys200=
XM_011523829.1:c.600A>G XP_011522131.1:p.Lys200=
XM_011523830.1:c.600A>G XP_011522132.1:p.Lys200=
XR_934021.1:n.707A>G
XR_934022.1:n.707A>G
XR_934023.1:n.707A>G
XM_006721516.3:c.600A>G XP_006721579.2:p.Lys200=
XM_011523829.2:c.600A>G XP_011522131.1:p.Lys200=
XM_011523830.2:c.600A>G XP_011522132.1:p.Lys200=
XM_024450741.1:c.600A>G XP_024306509.1:p.Lys200=
XR_934021.2:n.659A>G
XR_934022.2:n.659A>G
XR_934023.2:n.659A>G
NM_000018.4:c.600A>G MANE Select NP_000009.1:p.Lys200=
NM_001033859.3:c.534A>G NP_001029031.1:p.Lys178=
NM_001270447.2:c.669A>G NP_001257376.1:p.Lys223=
NM_001270448.2:c.372A>G NP_001257377.1:p.Lys124=