Canonical Allele Identifier: CA3047154175
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222868_7223134del , CM000679.2:g.7222868_7223134del GRCh38
NC_000017.10:g.7126187_7126453del , CM000679.1:g.7126187_7126453del GRCh37
NC_000017.9:g.7066911_7067177del NCBI36
NG_007975.1:g.8035_8301del
NG_008391.2:g.1920_2186del

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1077+3_1079del
ENST00000322910.9:c.*1032+3_*1034del
ENST00000350303.9:c.1011+3_1013del
ENST00000356839.9:c.1077+3_1079del
ENST00000543245.6:c.1146+3_1148del
ENST00000578824.5:n.229_495del
ENST00000582379.1:n.464_730del
ENST00000583858.5:c.106+3_108del
ENST00000585203.6:n.21_287del
NM_000018.3:c.1077+3_1079del
NM_001033859.2:c.1011+3_1013del
NM_001270447.1:c.1146+3_1148del
NM_001270448.1:c.849+3_851del
XM_006721516.2:c.1077+3_1079del
XM_011523829.1:c.1077+3_1079del
XM_011523830.1:c.1077+3_1079del
XR_934021.1:n.1184+3_1186del
XR_934022.1:n.1184+3_1186del
XR_934023.1:n.1184+3_1186del
XM_006721516.3:c.1077+3_1079del
XM_011523829.2:c.1077+3_1079del
XM_011523830.2:c.1077+3_1079del
XM_024450741.1:c.1077+3_1079del
XR_934021.2:n.1136+3_1138del
XR_934022.2:n.1136+3_1138del
XR_934023.2:n.1136+3_1138del
NM_000018.4:c.1077+3_1079del
NM_001033859.3:c.1011+3_1013del
NM_001270447.2:c.1146+3_1148del
NM_001270448.2:c.849+3_851del