Canonical Allele Identifier: CA2635781649
Gene: ACADVL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7223228_7223231del , CM000679.2:g.7223228_7223231del GRCh38
NC_000017.10:g.7126547_7126550del , CM000679.1:g.7126547_7126550del GRCh37
NC_000017.9:g.7067271_7067274del NCBI36
NG_007975.1:g.8395_8398del
NG_008391.2:g.1823_1826del

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1173_1176del MANE Select ENSP00000349297.5:p.Tyr391Ter
ENST00000322910.9:c.*1128_*1131del ENSP00000325395.5:n.*1128_*1131del
ENST00000350303.9:c.1107_1110del ENSP00000344152.5:p.Tyr369Ter
ENST00000356839.9:c.1173_1176del ENSP00000349297.5:p.Tyr391Ter
ENST00000542255.6:c.31_34del
ENST00000543245.6:c.1242_1245del ENSP00000438689.2:p.Tyr414Ter
ENST00000578579.2:n.122_125del
ENST00000578824.5:n.589_592del
ENST00000579425.5:n.197_200del
ENST00000579546.1:c.10_13del
ENST00000582379.1:n.824_827del
ENST00000583858.5:c.202_205del
ENST00000585203.6:n.381_384del
NM_000018.3:c.1173_1176del NP_000009.1:p.Tyr391Ter
NM_001033859.2:c.1107_1110del NP_001029031.1:p.Tyr369Ter
NM_001270447.1:c.1242_1245del NP_001257376.1:p.Tyr414Ter
NM_001270448.1:c.945_948del NP_001257377.1:p.Tyr315Ter
XM_006721516.2:c.1173_1176del XP_006721579.2:p.Tyr391Ter
XM_011523829.1:c.1173_1176del XP_011522131.1:p.Tyr391Ter
XM_011523830.1:c.1173_1176del XP_011522132.1:p.Tyr391Ter
XR_934021.1:n.1280_1283del
XR_934022.1:n.1280_1283del
XR_934023.1:n.1280_1283del
XM_006721516.3:c.1173_1176del XP_006721579.2:p.Tyr391Ter
XM_011523829.2:c.1173_1176del XP_011522131.1:p.Tyr391Ter
XM_011523830.2:c.1173_1176del XP_011522132.1:p.Tyr391Ter
XM_024450741.1:c.1173_1176del XP_024306509.1:p.Tyr391Ter
XR_934021.2:n.1232_1235del
XR_934022.2:n.1232_1235del
XR_934023.2:n.1232_1235del
NM_000018.4:c.1173_1176del MANE Select NP_000009.1:p.Tyr391Ter
NM_001033859.3:c.1107_1110del NP_001029031.1:p.Tyr369Ter
NM_001270447.2:c.1242_1245del NP_001257376.1:p.Tyr414Ter
NM_001270448.2:c.945_948del NP_001257377.1:p.Tyr315Ter