Canonical Allele Identifier: CA2739559235

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7219898T>C , CM000679.2:g.7219898T>C GRCh38
NC_000017.10:g.7123217T>C , CM000679.1:g.7123217T>C GRCh37
NC_000017.9:g.7063941T>C NCBI36
NG_007975.1:g.5065T>C
NG_008391.2:g.5153A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000322910.9:c.-87T>C (ACADVL) ENSP00000325395.5:n.-87T>C
ENST00000350303.9:c.-87T>C (ACADVL) ENSP00000344152.5:n.-87T>C
ENST00000356839.9:c.-87T>C (ACADVL) ENSP00000349297.5:n.-87T>C
ENST00000543245.6:c.132-224T>C (ACADVL) ENSP00000438689.2:n.132-224T>C
ENST00000577857.5:n.4T>C (ACADVL)
ENST00000578269.5:n.21T>C (ACADVL)
ENST00000579286.5:n.21T>C (ACADVL)
ENST00000580263.5:n.4T>C (ACADVL)
ENST00000582056.5:n.4T>C (ACADVL)
ENST00000582356.5:n.39T>C (ACADVL)
ENST00000583312.5:c.-87T>C (ACADVL) ENSP00000467920.1:n.-87T>C
NM_000018.3:c.-87T>C (ACADVL) NP_000009.1:n.-87T>C
NM_001033859.2:c.-87T>C (ACADVL) NP_001029031.1:n.-87T>C
NM_001270447.1:c.132-224T>C (ACADVL) NP_001257376.1:n.132-224T>C
NM_001270448.1:c.-390T>C (ACADVL) NP_001257377.1:n.-390T>C
NM_001365.3:c.-1049A>G (DLG4) NP_001356.1:n.-1049A>G
XM_006721516.2:c.-87T>C (ACADVL) XP_006721579.2:n.-87T>C
XM_011523829.1:c.-87T>C (ACADVL) XP_011522131.1:n.-87T>C
XM_011523830.1:c.-87T>C (ACADVL) XP_011522132.1:n.-87T>C
XR_934021.1:n.21T>C (ACADVL)
XR_934022.1:n.21T>C (ACADVL)
XR_934023.1:n.21T>C (ACADVL)
NM_001321074.1:c.-1049A>G (DLG4) NP_001308003.1:n.-1049A>G
NM_001365.4:c.-1049A>G (DLG4) NP_001356.1:n.-1049A>G
NR_135527.1:n.153A>G (DLG4)
NM_001270447.2:c.132-224T>C (ACADVL) NP_001257376.1:n.132-224T>C