Canonical Allele Identifier: CA2245697213

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7219854G= , CM000679.2:g.7219854G= GRCh38
NC_000017.10:g.7123173G= , CM000679.1:g.7123173G= GRCh37
NC_000017.9:g.7063897G= NCBI36
NG_007975.1:g.5021G=
NG_008391.2:g.5197C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000322910.9:c.-131G= (ACADVL) ENSP00000325395.5:n.-131G=
ENST00000356839.9:c.-131G= (ACADVL) ENSP00000349297.5:n.-131G=
ENST00000543245.6:c.132-268G= (ACADVL) ENSP00000438689.2:n.132-268G=
NM_000018.3:c.-131G= (ACADVL) NP_000009.1:n.-131G=
NM_001033859.2:c.-131G= (ACADVL) NP_001029031.1:n.-131G=
NM_001270447.1:c.132-268G= (ACADVL) NP_001257376.1:n.132-268G=
NM_001270448.1:c.-434G= (ACADVL) NP_001257377.1:n.-434G=
NM_001365.3:c.-1005C= (DLG4) NP_001356.1:n.-1005C=
NM_001321074.1:c.-1005C= (DLG4) NP_001308003.1:n.-1005C=
NM_001365.4:c.-1005C= (DLG4) NP_001356.1:n.-1005C=
NR_135527.1:n.197C= (DLG4)
NM_001270447.2:c.132-268G= (ACADVL) NP_001257376.1:n.132-268G=