Canonical Allele Identifier: CA397724773

Gene: ACADVL

Linked Data

• MyVariant Identifiers: chr17:g.7127145A>C (hg19) ; chr17:g.7223826A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7223826A>C , CM000679.2:g.7223826A>C	GRCh38
NC_000017.10:g.7127145A>C , CM000679.1:g.7127145A>C	GRCh37
NC_000017.9:g.7067869A>C	NCBI36
NG_007975.1:g.8993A>C
NG_008391.2:g.1225T>G
NG_033038.1:g.15719T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000356839.10:c.1283A>C MANE Select	ENSP00000349297.5:p.Lys428Thr
ENST00000322910.9:c.*1238A>C	ENSP00000325395.5:n.*1238A>C
ENST00000350303.9:c.1217A>C	ENSP00000344152.5:p.Lys406Thr
ENST00000356839.9:c.1283A>C	ENSP00000349297.5:p.Lys428Thr
ENST00000542255.6:c.141A>C
ENST00000543245.6:c.1352A>C	ENSP00000438689.2:p.Lys451Thr
ENST00000578579.2:n.454A>C
ENST00000578711.1:n.322A>C
ENST00000578824.5:n.699A>C
ENST00000579425.5:n.307A>C
ENST00000579546.1:c.120A>C
ENST00000583074.5:n.2A>C
ENST00000583850.5:n.58A>C
ENST00000583858.5:c.312A>C
ENST00000585203.6:n.491A>C
NM_000018.3:c.1283A>C	NP_000009.1:p.Lys428Thr
NM_001033859.2:c.1217A>C	NP_001029031.1:p.Lys406Thr
NM_001270447.1:c.1352A>C	NP_001257376.1:p.Lys451Thr
NM_001270448.1:c.1055A>C	NP_001257377.1:p.Lys352Thr
XM_006721516.2:c.1283A>C	XP_006721579.2:p.Lys428Thr
XM_011523829.1:c.1283A>C	XP_011522131.1:p.Lys428Thr
XM_011523830.1:c.1283A>C	XP_011522132.1:p.Lys428Thr
XR_934021.1:n.1390A>C
XR_934022.1:n.1390A>C
XR_934023.1:n.1390A>C
XM_006721516.3:c.1283A>C	XP_006721579.2:p.Lys428Thr
XM_011523829.2:c.1283A>C	XP_011522131.1:p.Lys428Thr
XM_011523830.2:c.1283A>C	XP_011522132.1:p.Lys428Thr
XM_024450741.1:c.1283A>C	XP_024306509.1:p.Lys428Thr
XR_934021.2:n.1342A>C
XR_934022.2:n.1342A>C
XR_934023.2:n.1342A>C
NM_000018.4:c.1283A>C MANE Select	NP_000009.1:p.Lys428Thr
NM_001033859.3:c.1217A>C	NP_001029031.1:p.Lys406Thr
NM_001270447.2:c.1352A>C	NP_001257376.1:p.Lys451Thr
NM_001270448.2:c.1055A>C	NP_001257377.1:p.Lys352Thr