Canonical Allele Identifier: CA2525034573
Gene: RANGRF HGNC NCBI
SLC25A35 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8288567_8288571del , CM000679.2:g.8288567_8288571del GRCh38
NC_000017.10:g.8191885_8191889del , CM000679.1:g.8191885_8191889del GRCh37
NC_000017.9:g.8132610_8132614del NCBI36
NG_028189.1:g.4917_4921del

Transcript Alleles

HGVS Amino-acid Change
ENST00000226105.10:c.-222_-218del (RANGRF) ENSP00000226105.6:n.-222_-218del
ENST00000380067.6:c.*1045_*1049del (SLC25A35) ENSP00000369407.2:n.*1045_*1049del
ENST00000579192.5:c.*43-139_*43-135del (SLC25A35) ENSP00000462395.1:n.*43-139_*43-135del
ENST00000581320.1:n.91-139_91-135del (SLC25A35)
NM_201520.1:c.*1045_*1049del (SLC25A35) NP_958928.1:n.*1045_*1049del
XM_005256618.3:c.-222_-218del (RANGRF) XP_005256675.1:n.-222_-218del
NM_001320871.1:c.*43-139_*43-135del (SLC25A35) NP_001307800.1:n.*43-139_*43-135del
NM_001330127.1:c.-222_-218del (RANGRF) NP_001317056.1:n.-222_-218del
NM_201520.2:c.*1045_*1049del (SLC25A35) NP_958928.1:n.*1045_*1049del
NM_001320871.2:c.*43-139_*43-135del (SLC25A35) NP_001307800.1:n.*43-139_*43-135del
NM_201520.3:c.*1045_*1049del (SLC25A35) NP_958928.1:n.*1045_*1049del
NR_135483.2:n.2590_2594del (SLC25A35)