Canonical Allele Identifier: CA2245699908
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7221494C= , CM000679.2:g.7221494C= GRCh38
NC_000017.10:g.7124813C= , CM000679.1:g.7124813C= GRCh37
NC_000017.9:g.7065537C= NCBI36
NG_007975.1:g.6661C=
NG_008391.2:g.3557G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.478-44C= MANE Select ENSP00000349297.5:n.478-44C=
ENST00000322910.9:c.*433-44C= ENSP00000325395.5:n.*433-44C=
ENST00000350303.9:c.412-44C= ENSP00000344152.5:n.412-44C=
ENST00000356839.9:c.478-44C= ENSP00000349297.5:n.478-44C=
ENST00000543245.6:c.547-44C= ENSP00000438689.2:n.547-44C=
ENST00000577191.5:n.555-44C=
ENST00000577433.5:n.686-44C=
ENST00000577857.5:n.294-44C=
ENST00000579286.5:n.659-44C=
ENST00000579886.2:c.316-44C= ENSP00000463246.1:n.316-44C=
ENST00000580365.1:n.209-44C=
ENST00000581378.5:c.177-25C=
ENST00000581562.5:n.524+436C=
ENST00000582166.1:n.459-44C=
ENST00000583312.5:c.478-44C= ENSP00000467920.1:n.478-44C=
ENST00000583760.1:n.216C=
NM_000018.3:c.478-44C= NP_000009.1:n.478-44C=
NM_001033859.2:c.412-44C= NP_001029031.1:n.412-44C=
NM_001270447.1:c.547-44C= NP_001257376.1:n.547-44C=
NM_001270448.1:c.250-44C= NP_001257377.1:n.250-44C=
XM_006721516.2:c.478-44C= XP_006721579.2:n.478-44C=
XM_011523829.1:c.478-44C= XP_011522131.1:n.478-44C=
XM_011523830.1:c.478-44C= XP_011522132.1:n.478-44C=
XR_934021.1:n.585-44C=
XR_934022.1:n.585-44C=
XR_934023.1:n.585-44C=
XM_006721516.3:c.478-44C= XP_006721579.2:n.478-44C=
XM_011523829.2:c.478-44C= XP_011522131.1:n.478-44C=
XM_011523830.2:c.478-44C= XP_011522132.1:n.478-44C=
XM_024450741.1:c.478-44C= XP_024306509.1:n.478-44C=
XR_934021.2:n.537-44C=
XR_934022.2:n.537-44C=
XR_934023.2:n.537-44C=
NM_000018.4:c.478-44C= MANE Select NP_000009.1:n.478-44C=
NM_001033859.3:c.412-44C= NP_001029031.1:n.412-44C=
NM_001270447.2:c.547-44C= NP_001257376.1:n.547-44C=
NM_001270448.2:c.250-44C= NP_001257377.1:n.250-44C=