Canonical Allele Identifier: CA2245713586

Gene: ACADVL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7224251_7224252delinsTA , CM000679.2:g.7224251_7224252delinsTA	GRCh38
NC_000017.10:g.7127570_7127571delinsTA , CM000679.1:g.7127570_7127571delinsTA	GRCh37
NC_000017.9:g.7068294_7068295delinsTA	NCBI36
NG_007975.1:g.9418_9419delinsTA
NG_008391.2:g.799_800delinsTA
NG_033038.1:g.15293_15294delinsTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000356839.10:c.1532+8_1532+9delinsTA MANE Select	ENSP00000349297.5:n.1532+8_1532+9delinsTA...
ENST00000322910.9:c.*1487+8_*1487+9delinsTA	ENSP00000325395.5:n.*1487+8_*1487+9delins...
ENST00000350303.9:c.1466+8_1466+9delinsTA	ENSP00000344152.5:n.1466+8_1466+9delinsTA...
ENST00000356839.9:c.1532+8_1532+9delinsTA	ENSP00000349297.5:n.1532+8_1532+9delinsTA...
ENST00000542255.6:c.390+8_390+9delinsTA
ENST00000543245.6:c.1601+8_1601+9delinsTA	ENSP00000438689.2:n.1601+8_1601+9delinsTA...
ENST00000578319.5:n.27+8_27+9delinsTA
ENST00000578711.1:n.747_748delinsTA
ENST00000578809.5:n.35_36delinsTA
ENST00000579391.1:n.140+8_140+9delinsTA
ENST00000579425.5:n.648+8_648+9delinsTA
ENST00000579546.1:c.272-70_272-69delinsTA
ENST00000579894.5:n.319+8_319+9delinsTA
ENST00000583074.5:n.154-70_154-69delinsTA
ENST00000583850.5:n.307+8_307+9delinsTA
ENST00000583858.5:c.464-70_464-69delinsTA
ENST00000585203.6:n.723+8_723+9delinsTA
NM_000018.3:c.1532+8_1532+9delinsTA	NP_000009.1:n.1532+8_1532+9delinsTA
NM_001033859.2:c.1466+8_1466+9delinsTA	NP_001029031.1:n.1466+8_1466+9delinsTA
NM_001270447.1:c.1601+8_1601+9delinsTA	NP_001257376.1:n.1601+8_1601+9delinsTA
NM_001270448.1:c.1304+8_1304+9delinsTA	NP_001257377.1:n.1304+8_1304+9delinsTA
XM_006721516.2:c.1532+8_1532+9delinsTA	XP_006721579.2:n.1532+8_1532+9delinsTA
XM_011523829.1:c.1435-70_1435-69delinsTA	XP_011522131.1:n.1435-70_1435-69delinsTA
XM_011523830.1:c.1435-70_1435-69delinsTA	XP_011522132.1:n.1435-70_1435-69delinsTA
XR_934021.1:n.1639+8_1639+9delinsTA
XR_934022.1:n.1542-70_1542-69delinsTA
XR_934023.1:n.1542-70_1542-69delinsTA
XM_006721516.3:c.1532+8_1532+9delinsTA	XP_006721579.2:n.1532+8_1532+9delinsTA
XM_011523829.2:c.1435-70_1435-69delinsTA	XP_011522131.1:n.1435-70_1435-69delinsTA
XM_011523830.2:c.1435-70_1435-69delinsTA	XP_011522132.1:n.1435-70_1435-69delinsTA
XM_024450741.1:c.1435-70_1435-69delinsTA	XP_024306509.1:n.1435-70_1435-69delinsTA
XR_934021.2:n.1591+8_1591+9delinsTA
XR_934022.2:n.1494-70_1494-69delinsTA
XR_934023.2:n.1494-70_1494-69delinsTA
NM_000018.4:c.1532+8_1532+9delinsTA MANE Select	NP_000009.1:n.1532+8_1532+9delinsTA
NM_001033859.3:c.1466+8_1466+9delinsTA	NP_001029031.1:n.1466+8_1466+9delinsTA
NM_001270447.2:c.1601+8_1601+9delinsTA	NP_001257376.1:n.1601+8_1601+9delinsTA
NM_001270448.2:c.1304+8_1304+9delinsTA	NP_001257377.1:n.1304+8_1304+9delinsTA