Canonical Allele Identifier: CA2245697221

Linked Data

dbSNP Id: rs2071095811

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7219866C>G , CM000679.2:g.7219866C>G GRCh38
NC_000017.10:g.7123185C>G , CM000679.1:g.7123185C>G GRCh37
NC_000017.9:g.7063909C>G NCBI36
NG_007975.1:g.5033C>G
NG_008391.2:g.5185G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000322910.9:c.-119C>G (ACADVL) ENSP00000325395.5:n.-119C>G
ENST00000350303.9:c.-119C>G (ACADVL) ENSP00000344152.5:n.-119C>G
ENST00000356839.9:c.-119C>G (ACADVL) ENSP00000349297.5:n.-119C>G
ENST00000543245.6:c.132-256C>G (ACADVL) ENSP00000438689.2:n.132-256C>G
ENST00000582356.5:n.7C>G (ACADVL)
ENST00000583312.5:c.-119C>G (ACADVL) ENSP00000467920.1:n.-119C>G
NM_000018.3:c.-119C>G (ACADVL) NP_000009.1:n.-119C>G
NM_001033859.2:c.-119C>G (ACADVL) NP_001029031.1:n.-119C>G
NM_001270447.1:c.132-256C>G (ACADVL) NP_001257376.1:n.132-256C>G
NM_001270448.1:c.-422C>G (ACADVL) NP_001257377.1:n.-422C>G
NM_001365.3:c.-1017G>C (DLG4) NP_001356.1:n.-1017G>C
NM_001321074.1:c.-1017G>C (DLG4) NP_001308003.1:n.-1017G>C
NM_001365.4:c.-1017G>C (DLG4) NP_001356.1:n.-1017G>C
NR_135527.1:n.185G>C (DLG4)
NM_001270447.2:c.132-256C>G (ACADVL) NP_001257376.1:n.132-256C>G