Canonical Allele Identifier: CA2635782822

Gene: ACADVL

Linked Data

• gnomAD v4: 17-7222609-T-TAGATCTCGGTGG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7222609_7222610insAGATCTCGGTGG , CM000679.2:g.7222609_7222610insAGATCTCGGTGG	GRCh38
NC_000017.10:g.7125928_7125929insAGATCTCGGTGG , CM000679.1:g.7125928_7125929insAGATCTCGGTGG	GRCh37
NC_000017.9:g.7066652_7066653insAGATCTCGGTGG	NCBI36
NG_007975.1:g.7776_7777insAGATCTCGGTGG
NG_008391.2:g.2441_2442insCCACCGAGATCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.879-58_879-57insAGATCTCGGTGG MANE Select	ENSP00000349297.5:n.879-58_879-57insAGATCTCGGTGG
ENST00000322910.9:c.*834-58_*834-57insAGATCTCGGTGG	ENSP00000325395.5:n.*834-58_*834-57insAGATCTCGGTGG
ENST00000350303.9:c.813-58_813-57insAGATCTCGGTGG	ENSP00000344152.5:n.813-58_813-57insAGATCTCGGTGG
ENST00000356839.9:c.879-58_879-57insAGATCTCGGTGG	ENSP00000349297.5:n.879-58_879-57insAGATCTCGGTGG
ENST00000543245.6:c.948-58_948-57insAGATCTCGGTGG	ENSP00000438689.2:n.948-58_948-57insAGATCTCGGTGG
ENST00000581378.5:c.597-58_597-57insAGATCTCGGTGG
ENST00000582379.1:n.263-58_263-57insAGATCTCGGTGG
NM_000018.3:c.879-58_879-57insAGATCTCGGTGG	NP_000009.1:n.879-58_879-57insAGATCTCGGTGG
NM_001033859.2:c.813-58_813-57insAGATCTCGGTGG	NP_001029031.1:n.813-58_813-57insAGATCTCGGTGG
NM_001270447.1:c.948-58_948-57insAGATCTCGGTGG	NP_001257376.1:n.948-58_948-57insAGATCTCGGTGG
NM_001270448.1:c.651-58_651-57insAGATCTCGGTGG	NP_001257377.1:n.651-58_651-57insAGATCTCGGTGG
XM_006721516.2:c.879-58_879-57insAGATCTCGGTGG	XP_006721579.2:n.879-58_879-57insAGATCTCGGTGG
XM_011523829.1:c.879-58_879-57insAGATCTCGGTGG	XP_011522131.1:n.879-58_879-57insAGATCTCGGTGG
XM_011523830.1:c.879-58_879-57insAGATCTCGGTGG	XP_011522132.1:n.879-58_879-57insAGATCTCGGTGG
XR_934021.1:n.986-58_986-57insAGATCTCGGTGG
XR_934022.1:n.986-58_986-57insAGATCTCGGTGG
XR_934023.1:n.986-58_986-57insAGATCTCGGTGG
XM_006721516.3:c.879-58_879-57insAGATCTCGGTGG	XP_006721579.2:n.879-58_879-57insAGATCTCGGTGG
XM_011523829.2:c.879-58_879-57insAGATCTCGGTGG	XP_011522131.1:n.879-58_879-57insAGATCTCGGTGG
XM_011523830.2:c.879-58_879-57insAGATCTCGGTGG	XP_011522132.1:n.879-58_879-57insAGATCTCGGTGG
XM_024450741.1:c.879-58_879-57insAGATCTCGGTGG	XP_024306509.1:n.879-58_879-57insAGATCTCGGTGG
XR_934021.2:n.938-58_938-57insAGATCTCGGTGG
XR_934022.2:n.938-58_938-57insAGATCTCGGTGG
XR_934023.2:n.938-58_938-57insAGATCTCGGTGG
NM_000018.4:c.879-58_879-57insAGATCTCGGTGG MANE Select	NP_000009.1:n.879-58_879-57insAGATCTCGGTGG
NM_001033859.3:c.813-58_813-57insAGATCTCGGTGG	NP_001029031.1:n.813-58_813-57insAGATCTCGGTGG
NM_001270447.2:c.948-58_948-57insAGATCTCGGTGG	NP_001257376.1:n.948-58_948-57insAGATCTCGGTGG
NM_001270448.2:c.651-58_651-57insAGATCTCGGTGG	NP_001257377.1:n.651-58_651-57insAGATCTCGGTGG