Canonical Allele Identifier: CA2635778096

Linked Data

gnomAD v4: 17-7219855-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7219855G>A , CM000679.2:g.7219855G>A GRCh38
NC_000017.10:g.7123174G>A , CM000679.1:g.7123174G>A GRCh37
NC_000017.9:g.7063898G>A NCBI36
NG_007975.1:g.5022G>A
NG_008391.2:g.5196C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000322910.9:c.-130G>A (ACADVL) ENSP00000325395.5:n.-130G>A
ENST00000356839.9:c.-130G>A (ACADVL) ENSP00000349297.5:n.-130G>A
ENST00000543245.6:c.132-267G>A (ACADVL) ENSP00000438689.2:n.132-267G>A
NM_000018.3:c.-130G>A (ACADVL) NP_000009.1:n.-130G>A
NM_001033859.2:c.-130G>A (ACADVL) NP_001029031.1:n.-130G>A
NM_001270447.1:c.132-267G>A (ACADVL) NP_001257376.1:n.132-267G>A
NM_001270448.1:c.-433G>A (ACADVL) NP_001257377.1:n.-433G>A
NM_001365.3:c.-1006C>T (DLG4) NP_001356.1:n.-1006C>T
NM_001321074.1:c.-1006C>T (DLG4) NP_001308003.1:n.-1006C>T
NM_001365.4:c.-1006C>T (DLG4) NP_001356.1:n.-1006C>T
NR_135527.1:n.196C>T (DLG4)
NM_001270447.2:c.132-267G>A (ACADVL) NP_001257376.1:n.132-267G>A