Canonical Allele Identifier: CA2245697214

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7219856G= , CM000679.2:g.7219856G= GRCh38
NC_000017.10:g.7123175G= , CM000679.1:g.7123175G= GRCh37
NC_000017.9:g.7063899G= NCBI36
NG_007975.1:g.5023G=
NG_008391.2:g.5195C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000322910.9:c.-129G= (ACADVL) ENSP00000325395.5:n.-129G=
ENST00000356839.9:c.-129G= (ACADVL) ENSP00000349297.5:n.-129G=
ENST00000543245.6:c.132-266G= (ACADVL) ENSP00000438689.2:n.132-266G=
NM_000018.3:c.-129G= (ACADVL) NP_000009.1:n.-129G=
NM_001033859.2:c.-129G= (ACADVL) NP_001029031.1:n.-129G=
NM_001270447.1:c.132-266G= (ACADVL) NP_001257376.1:n.132-266G=
NM_001270448.1:c.-432G= (ACADVL) NP_001257377.1:n.-432G=
NM_001365.3:c.-1007C= (DLG4) NP_001356.1:n.-1007C=
NM_001321074.1:c.-1007C= (DLG4) NP_001308003.1:n.-1007C=
NM_001365.4:c.-1007C= (DLG4) NP_001356.1:n.-1007C=
NR_135527.1:n.195C= (DLG4)
NM_001270447.2:c.132-266G= (ACADVL) NP_001257376.1:n.132-266G=