Canonical Allele Identifier: CA2635778123

Linked Data

gnomAD v4: 17-7219862-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7219862C>A , CM000679.2:g.7219862C>A GRCh38
NC_000017.10:g.7123181C>A , CM000679.1:g.7123181C>A GRCh37
NC_000017.9:g.7063905C>A NCBI36
NG_007975.1:g.5029C>A
NG_008391.2:g.5189G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000322910.9:c.-123C>A (ACADVL) ENSP00000325395.5:n.-123C>A
ENST00000356839.9:c.-123C>A (ACADVL) ENSP00000349297.5:n.-123C>A
ENST00000543245.6:c.132-260C>A (ACADVL) ENSP00000438689.2:n.132-260C>A
ENST00000582356.5:n.3C>A (ACADVL)
ENST00000583312.5:c.-123C>A (ACADVL) ENSP00000467920.1:n.-123C>A
NM_000018.3:c.-123C>A (ACADVL) NP_000009.1:n.-123C>A
NM_001033859.2:c.-123C>A (ACADVL) NP_001029031.1:n.-123C>A
NM_001270447.1:c.132-260C>A (ACADVL) NP_001257376.1:n.132-260C>A
NM_001270448.1:c.-426C>A (ACADVL) NP_001257377.1:n.-426C>A
NM_001365.3:c.-1013G>T (DLG4) NP_001356.1:n.-1013G>T
NM_001321074.1:c.-1013G>T (DLG4) NP_001308003.1:n.-1013G>T
NM_001365.4:c.-1013G>T (DLG4) NP_001356.1:n.-1013G>T
NR_135527.1:n.189G>T (DLG4)
NM_001270447.2:c.132-260C>A (ACADVL) NP_001257376.1:n.132-260C>A