Canonical Allele Identifier: CA2245697231

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7219875C= , CM000679.2:g.7219875C= GRCh38
NC_000017.10:g.7123194C= , CM000679.1:g.7123194C= GRCh37
NC_000017.9:g.7063918C= NCBI36
NG_007975.1:g.5042C=
NG_008391.2:g.5176G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000322910.9:c.-110C= (ACADVL) ENSP00000325395.5:n.-110C=
ENST00000350303.9:c.-110C= (ACADVL) ENSP00000344152.5:n.-110C=
ENST00000356839.9:c.-110C= (ACADVL) ENSP00000349297.5:n.-110C=
ENST00000543245.6:c.132-247C= (ACADVL) ENSP00000438689.2:n.132-247C=
ENST00000582356.5:n.16C= (ACADVL)
ENST00000583312.5:c.-110C= (ACADVL) ENSP00000467920.1:n.-110C=
NM_000018.3:c.-110C= (ACADVL) NP_000009.1:n.-110C=
NM_001033859.2:c.-110C= (ACADVL) NP_001029031.1:n.-110C=
NM_001270447.1:c.132-247C= (ACADVL) NP_001257376.1:n.132-247C=
NM_001270448.1:c.-413C= (ACADVL) NP_001257377.1:n.-413C=
NM_001365.3:c.-1026G= (DLG4) NP_001356.1:n.-1026G=
NM_001321074.1:c.-1026G= (DLG4) NP_001308003.1:n.-1026G=
NM_001365.4:c.-1026G= (DLG4) NP_001356.1:n.-1026G=
NR_135527.1:n.176G= (DLG4)
NM_001270447.2:c.132-247C= (ACADVL) NP_001257376.1:n.132-247C=