Canonical Allele Identifier: CA2635778151

Linked Data

gnomAD v4: 17-7219871-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7219871G>T , CM000679.2:g.7219871G>T GRCh38
NC_000017.10:g.7123190G>T , CM000679.1:g.7123190G>T GRCh37
NC_000017.9:g.7063914G>T NCBI36
NG_007975.1:g.5038G>T
NG_008391.2:g.5180C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000322910.9:c.-114G>T (ACADVL) ENSP00000325395.5:n.-114G>T
ENST00000350303.9:c.-114G>T (ACADVL) ENSP00000344152.5:n.-114G>T
ENST00000356839.9:c.-114G>T (ACADVL) ENSP00000349297.5:n.-114G>T
ENST00000543245.6:c.132-251G>T (ACADVL) ENSP00000438689.2:n.132-251G>T
ENST00000582356.5:n.12G>T (ACADVL)
ENST00000583312.5:c.-114G>T (ACADVL) ENSP00000467920.1:n.-114G>T
NM_000018.3:c.-114G>T (ACADVL) NP_000009.1:n.-114G>T
NM_001033859.2:c.-114G>T (ACADVL) NP_001029031.1:n.-114G>T
NM_001270447.1:c.132-251G>T (ACADVL) NP_001257376.1:n.132-251G>T
NM_001270448.1:c.-417G>T (ACADVL) NP_001257377.1:n.-417G>T
NM_001365.3:c.-1022C>A (DLG4) NP_001356.1:n.-1022C>A
NM_001321074.1:c.-1022C>A (DLG4) NP_001308003.1:n.-1022C>A
NM_001365.4:c.-1022C>A (DLG4) NP_001356.1:n.-1022C>A
NR_135527.1:n.180C>A (DLG4)
NM_001270447.2:c.132-251G>T (ACADVL) NP_001257376.1:n.132-251G>T