Canonical Allele Identifier: CA397724879

Gene: ACADVL

Linked Data

• ClinVar Variation Id: 1437726
• ClinVar RCV Id: RCV001934084
• dbSNP Id: rs886043236
• gnomAD v2: 17-7127190-T-C
• gnomAD v4: 17-7223871-T-C
• MyVariant Identifiers: chr17:g.7127190T>C (hg19) ; chr17:g.7223871T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7223871T>C , CM000679.2:g.7223871T>C	GRCh38
NC_000017.10:g.7127190T>C , CM000679.1:g.7127190T>C	GRCh37
NC_000017.9:g.7067914T>C	NCBI36
NG_007975.1:g.9038T>C
NG_008391.2:g.1180A>G
NG_033038.1:g.15674A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1328T>C MANE Select	ENSP00000349297.5:p.Met443Thr
ENST00000322910.9:c.*1283T>C	ENSP00000325395.5:n.*1283T>C
ENST00000350303.9:c.1262T>C	ENSP00000344152.5:p.Met421Thr
ENST00000356839.9:c.1328T>C	ENSP00000349297.5:p.Met443Thr
ENST00000542255.6:c.186T>C
ENST00000543245.6:c.1397T>C	ENSP00000438689.2:p.Met466Thr
ENST00000578711.1:n.367T>C
ENST00000579425.5:n.352T>C
ENST00000579546.1:c.165T>C
ENST00000583074.5:n.47T>C
ENST00000583850.5:n.103T>C
ENST00000583858.5:c.357T>C
ENST00000585203.6:n.523+13T>C
NM_000018.3:c.1328T>C	NP_000009.1:p.Met443Thr
NM_001033859.2:c.1262T>C	NP_001029031.1:p.Met421Thr
NM_001270447.1:c.1397T>C	NP_001257376.1:p.Met466Thr
NM_001270448.1:c.1100T>C	NP_001257377.1:p.Met367Thr
XM_006721516.2:c.1328T>C	XP_006721579.2:p.Met443Thr
XM_011523829.1:c.1328T>C	XP_011522131.1:p.Met443Thr
XM_011523830.1:c.1328T>C	XP_011522132.1:p.Met443Thr
XR_934021.1:n.1435T>C
XR_934022.1:n.1435T>C
XR_934023.1:n.1435T>C
XM_006721516.3:c.1328T>C	XP_006721579.2:p.Met443Thr
XM_011523829.2:c.1328T>C	XP_011522131.1:p.Met443Thr
XM_011523830.2:c.1328T>C	XP_011522132.1:p.Met443Thr
XM_024450741.1:c.1328T>C	XP_024306509.1:p.Met443Thr
XR_934021.2:n.1387T>C
XR_934022.2:n.1387T>C
XR_934023.2:n.1387T>C
NM_000018.4:c.1328T>C MANE Select	NP_000009.1:p.Met443Thr
NM_001033859.3:c.1262T>C	NP_001029031.1:p.Met421Thr
NM_001270447.2:c.1397T>C	NP_001257376.1:p.Met466Thr
NM_001270448.2:c.1100T>C	NP_001257377.1:p.Met367Thr