Canonical Allele Identifier: CA397724770

Gene: ACADVL

Linked Data

• MyVariant Identifiers: chr17:g.7127144A>C (hg19) ; chr17:g.7223825A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7223825A>C , CM000679.2:g.7223825A>C	GRCh38
NC_000017.10:g.7127144A>C , CM000679.1:g.7127144A>C	GRCh37
NC_000017.9:g.7067868A>C	NCBI36
NG_007975.1:g.8992A>C
NG_008391.2:g.1226T>G
NG_033038.1:g.15720T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1282A>C MANE Select	ENSP00000349297.5:p.Lys428Gln
ENST00000322910.9:c.*1237A>C	ENSP00000325395.5:n.*1237A>C
ENST00000350303.9:c.1216A>C	ENSP00000344152.5:p.Lys406Gln
ENST00000356839.9:c.1282A>C	ENSP00000349297.5:p.Lys428Gln
ENST00000542255.6:c.140A>C
ENST00000543245.6:c.1351A>C	ENSP00000438689.2:p.Lys451Gln
ENST00000578579.2:n.453A>C
ENST00000578711.1:n.321A>C
ENST00000578824.5:n.698A>C
ENST00000579425.5:n.306A>C
ENST00000579546.1:c.119A>C
ENST00000583074.5:n.1A>C
ENST00000583850.5:n.57A>C
ENST00000583858.5:c.311A>C
ENST00000585203.6:n.490A>C
NM_000018.3:c.1282A>C	NP_000009.1:p.Lys428Gln
NM_001033859.2:c.1216A>C	NP_001029031.1:p.Lys406Gln
NM_001270447.1:c.1351A>C	NP_001257376.1:p.Lys451Gln
NM_001270448.1:c.1054A>C	NP_001257377.1:p.Lys352Gln
XM_006721516.2:c.1282A>C	XP_006721579.2:p.Lys428Gln
XM_011523829.1:c.1282A>C	XP_011522131.1:p.Lys428Gln
XM_011523830.1:c.1282A>C	XP_011522132.1:p.Lys428Gln
XR_934021.1:n.1389A>C
XR_934022.1:n.1389A>C
XR_934023.1:n.1389A>C
XM_006721516.3:c.1282A>C	XP_006721579.2:p.Lys428Gln
XM_011523829.2:c.1282A>C	XP_011522131.1:p.Lys428Gln
XM_011523830.2:c.1282A>C	XP_011522132.1:p.Lys428Gln
XM_024450741.1:c.1282A>C	XP_024306509.1:p.Lys428Gln
XR_934021.2:n.1341A>C
XR_934022.2:n.1341A>C
XR_934023.2:n.1341A>C
NM_000018.4:c.1282A>C MANE Select	NP_000009.1:p.Lys428Gln
NM_001033859.3:c.1216A>C	NP_001029031.1:p.Lys406Gln
NM_001270447.2:c.1351A>C	NP_001257376.1:p.Lys451Gln
NM_001270448.2:c.1054A>C	NP_001257377.1:p.Lys352Gln