Canonical Allele Identifier: CA2635780967
Gene: ACADVL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221398_7221399del , CM000679.2:g.7221398_7221399del GRCh38
NC_000017.10:g.7124717_7124718del , CM000679.1:g.7124717_7124718del GRCh37
NC_000017.9:g.7065441_7065442del NCBI36
NG_007975.1:g.6565_6566del
NG_008391.2:g.3656_3657del

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.478-140_478-139del MANE Select ENSP00000349297.5:n.478-140_478-139del
ENST00000322910.9:c.*433-140_*433-139del ENSP00000325395.5:n.*433-140_*433-139del
ENST00000350303.9:c.412-140_412-139del ENSP00000344152.5:n.412-140_412-139del
ENST00000356839.9:c.478-140_478-139del ENSP00000349297.5:n.478-140_478-139del
ENST00000543245.6:c.547-140_547-139del ENSP00000438689.2:n.547-140_547-139del
ENST00000577191.5:n.555-140_555-139del
ENST00000577433.5:n.686-140_686-139del
ENST00000577857.5:n.294-140_294-139del
ENST00000579286.5:n.659-140_659-139del
ENST00000579886.2:c.316-140_316-139del ENSP00000463246.1:n.316-140_316-139del
ENST00000580365.1:n.209-140_209-139del
ENST00000581378.5:c.177-121_177-120del
ENST00000581562.5:n.524+340_524+341del
ENST00000582166.1:n.459-140_459-139del
ENST00000583312.5:c.478-140_478-139del ENSP00000467920.1:n.478-140_478-139del
ENST00000583760.1:n.120_121del
NM_000018.3:c.478-140_478-139del NP_000009.1:n.478-140_478-139del
NM_001033859.2:c.412-140_412-139del NP_001029031.1:n.412-140_412-139del
NM_001270447.1:c.547-140_547-139del NP_001257376.1:n.547-140_547-139del
NM_001270448.1:c.250-140_250-139del NP_001257377.1:n.250-140_250-139del
XM_006721516.2:c.478-140_478-139del XP_006721579.2:n.478-140_478-139del
XM_011523829.1:c.478-140_478-139del XP_011522131.1:n.478-140_478-139del
XM_011523830.1:c.478-140_478-139del XP_011522132.1:n.478-140_478-139del
XR_934021.1:n.585-140_585-139del
XR_934022.1:n.585-140_585-139del
XR_934023.1:n.585-140_585-139del
XM_006721516.3:c.478-140_478-139del XP_006721579.2:n.478-140_478-139del
XM_011523829.2:c.478-140_478-139del XP_011522131.1:n.478-140_478-139del
XM_011523830.2:c.478-140_478-139del XP_011522132.1:n.478-140_478-139del
XM_024450741.1:c.478-140_478-139del XP_024306509.1:n.478-140_478-139del
XR_934021.2:n.537-140_537-139del
XR_934022.2:n.537-140_537-139del
XR_934023.2:n.537-140_537-139del
NM_000018.4:c.478-140_478-139del MANE Select NP_000009.1:n.478-140_478-139del
NM_001033859.3:c.412-140_412-139del NP_001029031.1:n.412-140_412-139del
NM_001270447.2:c.547-140_547-139del NP_001257376.1:n.547-140_547-139del
NM_001270448.2:c.250-140_250-139del NP_001257377.1:n.250-140_250-139del