Canonical Allele Identifier: CA2635781394
Gene: ACADVL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221737_7221812dup , CM000679.2:g.7221737_7221812dup GRCh38
NC_000017.10:g.7125056_7125131dup , CM000679.1:g.7125056_7125131dup GRCh37
NC_000017.9:g.7065780_7065855dup NCBI36
NG_007975.1:g.6904_6979dup
NG_008391.2:g.3244_3319dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.622+55_622+130dup MANE Select ENSP00000349297.5:n.622+55_622+130dup
ENST00000322910.9:c.*577+55_*577+130dup ENSP00000325395.5:n.*577+55_*577+130dup
ENST00000350303.9:c.556+55_556+130dup ENSP00000344152.5:n.556+55_556+130dup
ENST00000356839.9:c.622+55_622+130dup ENSP00000349297.5:n.622+55_622+130dup
ENST00000543245.6:c.691+55_691+130dup ENSP00000438689.2:n.691+55_691+130dup
ENST00000577191.5:n.699+55_699+130dup
ENST00000577857.5:n.438+55_438+130dup
ENST00000579286.5:n.803+55_803+130dup
ENST00000579886.2:c.460+55_460+130dup ENSP00000463246.1:n.460+55_460+130dup
ENST00000580365.1:n.353+55_353+130dup
ENST00000581378.5:c.340+55_340+130dup
ENST00000581562.5:n.525-215_525-140dup
ENST00000583312.5:c.622+55_623-125dup ENSP00000467920.1:n.622+55_623-125dup
ENST00000583760.1:n.404+55_404+130dup
NM_000018.3:c.622+55_622+130dup NP_000009.1:n.622+55_622+130dup
NM_001033859.2:c.556+55_556+130dup NP_001029031.1:n.556+55_556+130dup
NM_001270447.1:c.691+55_691+130dup NP_001257376.1:n.691+55_691+130dup
NM_001270448.1:c.394+55_394+130dup NP_001257377.1:n.394+55_394+130dup
XM_006721516.2:c.622+55_622+130dup XP_006721579.2:n.622+55_622+130dup
XM_011523829.1:c.622+55_622+130dup XP_011522131.1:n.622+55_622+130dup
XM_011523830.1:c.622+55_622+130dup XP_011522132.1:n.622+55_622+130dup
XR_934021.1:n.729+55_729+130dup
XR_934022.1:n.729+55_729+130dup
XR_934023.1:n.729+55_729+130dup
XM_006721516.3:c.622+55_622+130dup XP_006721579.2:n.622+55_622+130dup
XM_011523829.2:c.622+55_622+130dup XP_011522131.1:n.622+55_622+130dup
XM_011523830.2:c.622+55_622+130dup XP_011522132.1:n.622+55_622+130dup
XM_024450741.1:c.622+55_622+130dup XP_024306509.1:n.622+55_622+130dup
XR_934021.2:n.681+55_681+130dup
XR_934022.2:n.681+55_681+130dup
XR_934023.2:n.681+55_681+130dup
NM_000018.4:c.622+55_622+130dup MANE Select NP_000009.1:n.622+55_622+130dup
NM_001033859.3:c.556+55_556+130dup NP_001029031.1:n.556+55_556+130dup
NM_001270447.2:c.691+55_691+130dup NP_001257376.1:n.691+55_691+130dup
NM_001270448.2:c.394+55_394+130dup NP_001257377.1:n.394+55_394+130dup