Canonical Allele Identifier: CA2635993391
Gene: RANGRF HGNC NCBI
SLC25A35 HGNC NCBI

Linked Data

gnomAD v4: 17-8288643-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8288643A>T , CM000679.2:g.8288643A>T GRCh38
NC_000017.10:g.8191961A>T , CM000679.1:g.8191961A>T GRCh37
NC_000017.9:g.8132686A>T NCBI36
NG_028189.1:g.4993A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000226105.10:c.-146A>T (RANGRF) ENSP00000226105.6:n.-146A>T
ENST00000380067.6:c.*973T>A (SLC25A35) ENSP00000369407.2:n.*973T>A
ENST00000579192.5:c.*43-211T>A (SLC25A35) ENSP00000462395.1:n.*43-211T>A
ENST00000581320.1:n.91-211T>A (SLC25A35)
NM_201520.1:c.*973T>A (SLC25A35) NP_958928.1:n.*973T>A
XM_005256618.3:c.-146A>T (RANGRF) XP_005256675.1:n.-146A>T
NM_001320871.1:c.*43-211T>A (SLC25A35) NP_001307800.1:n.*43-211T>A
NM_001330127.1:c.-146A>T (RANGRF) NP_001317056.1:n.-146A>T
NM_201520.2:c.*973T>A (SLC25A35) NP_958928.1:n.*973T>A
NM_001320871.2:c.*43-211T>A (SLC25A35) NP_001307800.1:n.*43-211T>A
NM_201520.3:c.*973T>A (SLC25A35) NP_958928.1:n.*973T>A
NR_135483.2:n.2518T>A (SLC25A35)