Canonical Allele Identifier: CA2245699849
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221453_7221454delinsGA , CM000679.2:g.7221453_7221454delinsGA GRCh38
NC_000017.10:g.7124772_7124773delinsGA , CM000679.1:g.7124772_7124773delinsGA GRCh37
NC_000017.9:g.7065496_7065497delinsGA NCBI36
NG_007975.1:g.6620_6621delinsGA
NG_008391.2:g.3597_3598delinsTC

Transcript Alleles

HGVS Amino-acid change
ENST00000356839.10:c.478-85_478-84delinsGA MANE Select ENSP00000349297.5:n.478-85_478-84delinsGA
ENST00000322910.9:c.*433-85_*433-84delinsGA ENSP00000325395.5:n.*433-85_*433-84delinsGA
ENST00000350303.9:c.412-85_412-84delinsGA ENSP00000344152.5:n.412-85_412-84delinsGA
ENST00000356839.9:c.478-85_478-84delinsGA ENSP00000349297.5:n.478-85_478-84delinsGA
ENST00000543245.6:c.547-85_547-84delinsGA ENSP00000438689.2:n.547-85_547-84delinsGA
ENST00000577191.5:n.555-85_555-84delinsGA
ENST00000577433.5:n.686-85_686-84delinsGA
ENST00000577857.5:n.294-85_294-84delinsGA
ENST00000579286.5:n.659-85_659-84delinsGA
ENST00000579886.2:c.316-85_316-84delinsGA ENSP00000463246.1:n.316-85_316-84delinsGA
ENST00000580365.1:n.209-85_209-84delinsGA
ENST00000581378.5:c.177-66_177-65delinsGA
ENST00000581562.5:n.524+395_524+396delinsGA
ENST00000582166.1:n.459-85_459-84delinsGA
ENST00000583312.5:c.478-85_478-84delinsGA ENSP00000467920.1:n.478-85_478-84delinsGA
ENST00000583760.1:n.175_176delinsGA
NM_000018.3:c.478-85_478-84delinsGA NP_000009.1:n.478-85_478-84delinsGA
NM_001033859.2:c.412-85_412-84delinsGA NP_001029031.1:n.412-85_412-84delinsGA
NM_001270447.1:c.547-85_547-84delinsGA NP_001257376.1:n.547-85_547-84delinsGA
NM_001270448.1:c.250-85_250-84delinsGA NP_001257377.1:n.250-85_250-84delinsGA
XM_006721516.2:c.478-85_478-84delinsGA XP_006721579.2:n.478-85_478-84delinsGA
XM_011523829.1:c.478-85_478-84delinsGA XP_011522131.1:n.478-85_478-84delinsGA
XM_011523830.1:c.478-85_478-84delinsGA XP_011522132.1:n.478-85_478-84delinsGA
XR_934021.1:n.585-85_585-84delinsGA
XR_934022.1:n.585-85_585-84delinsGA
XR_934023.1:n.585-85_585-84delinsGA
XM_006721516.3:c.478-85_478-84delinsGA XP_006721579.2:n.478-85_478-84delinsGA
XM_011523829.2:c.478-85_478-84delinsGA XP_011522131.1:n.478-85_478-84delinsGA
XM_011523830.2:c.478-85_478-84delinsGA XP_011522132.1:n.478-85_478-84delinsGA
XM_024450741.1:c.478-85_478-84delinsGA XP_024306509.1:n.478-85_478-84delinsGA
XR_934021.2:n.537-85_537-84delinsGA
XR_934022.2:n.537-85_537-84delinsGA
XR_934023.2:n.537-85_537-84delinsGA
NM_000018.4:c.478-85_478-84delinsGA MANE Select NP_000009.1:n.478-85_478-84delinsGA
NM_001033859.3:c.412-85_412-84delinsGA NP_001029031.1:n.412-85_412-84delinsGA
NM_001270447.2:c.547-85_547-84delinsGA NP_001257376.1:n.547-85_547-84delinsGA
NM_001270448.2:c.250-85_250-84delinsGA NP_001257377.1:n.250-85_250-84delinsGA