Canonical Allele Identifier: CA2245714060

Gene: ACADVL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7224399_7224400delinsTG , CM000679.2:g.7224399_7224400delinsTG	GRCh38
NC_000017.10:g.7127718_7127719delinsTG , CM000679.1:g.7127718_7127719delinsTG	GRCh37
NC_000017.9:g.7068442_7068443delinsTG	NCBI36
NG_007975.1:g.9566_9567delinsTG
NG_008391.2:g.651_652delinsCA
NG_033038.1:g.15145_15146delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1605+6_1605+7delinsTG MANE Select	ENSP00000349297.5:n.1605+6_1605+7delinsTG
ENST00000322910.9:c.*1560+6_*1560+7delinsTG	ENSP00000325395.5:n.*1560+6_*1560+7delinsTG
ENST00000350303.9:c.1539+6_1539+7delinsTG	ENSP00000344152.5:n.1539+6_1539+7delinsTG
ENST00000356839.9:c.1605+6_1605+7delinsTG	ENSP00000349297.5:n.1605+6_1605+7delinsTG
ENST00000542255.6:c.463+6_463+7delinsTG
ENST00000543245.6:c.1674+6_1674+7delinsTG	ENSP00000438689.2:n.1674+6_1674+7delinsTG
ENST00000578319.5:n.106_107delinsTG
ENST00000578711.1:n.895_896delinsTG
ENST00000578809.5:n.177+6_177+7delinsTG
ENST00000579391.1:n.213+6_213+7delinsTG
ENST00000579425.5:n.721+6_721+7delinsTG
ENST00000579546.1:c.344+6_344+7delinsTG
ENST00000579894.5:n.392+6_392+7delinsTG
ENST00000582450.1:n.113+6_113+7delinsTG
ENST00000583074.5:n.226+6_226+7delinsTG
ENST00000583850.5:n.380+6_380+7delinsTG
ENST00000583858.5:c.536+6_536+7delinsTG
ENST00000585203.6:n.796+6_796+7delinsTG
NM_000018.3:c.1605+6_1605+7delinsTG	NP_000009.1:n.1605+6_1605+7delinsTG
NM_001033859.2:c.1539+6_1539+7delinsTG	NP_001029031.1:n.1539+6_1539+7delinsTG
NM_001270447.1:c.1674+6_1674+7delinsTG	NP_001257376.1:n.1674+6_1674+7delinsTG
NM_001270448.1:c.1377+6_1377+7delinsTG	NP_001257377.1:n.1377+6_1377+7delinsTG
XM_006721516.2:c.1605+6_1605+7delinsTG	XP_006721579.2:n.1605+6_1605+7delinsTG
XM_011523829.1:c.1507+6_1507+7delinsTG	XP_011522131.1:n.1507+6_1507+7delinsTG
XM_011523830.1:c.1507+6_1507+7delinsTG	XP_011522132.1:n.1507+6_1507+7delinsTG
XR_934021.1:n.1712+6_1712+7delinsTG
XR_934022.1:n.1614+6_1614+7delinsTG
XR_934023.1:n.1614+6_1614+7delinsTG
XM_006721516.3:c.1605+6_1605+7delinsTG	XP_006721579.2:n.1605+6_1605+7delinsTG
XM_011523829.2:c.1507+6_1507+7delinsTG	XP_011522131.1:n.1507+6_1507+7delinsTG
XM_011523830.2:c.1507+6_1507+7delinsTG	XP_011522132.1:n.1507+6_1507+7delinsTG
XM_024450741.1:c.1513_1514delinsTG	XP_024306509.1:p.Trp505=
XR_934021.2:n.1664+6_1664+7delinsTG
XR_934022.2:n.1566+6_1566+7delinsTG
XR_934023.2:n.1566+6_1566+7delinsTG
NM_000018.4:c.1605+6_1605+7delinsTG MANE Select	NP_000009.1:n.1605+6_1605+7delinsTG
NM_001033859.3:c.1539+6_1539+7delinsTG	NP_001029031.1:n.1539+6_1539+7delinsTG
NM_001270447.2:c.1674+6_1674+7delinsTG	NP_001257376.1:n.1674+6_1674+7delinsTG
NM_001270448.2:c.1377+6_1377+7delinsTG	NP_001257377.1:n.1377+6_1377+7delinsTG