Canonical Allele Identifier: CA2635993412
Gene: RANGRF HGNC NCBI
SLC25A35 HGNC NCBI

Linked Data

gnomAD v4: 17-8288654-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8288654A>G , CM000679.2:g.8288654A>G GRCh38
NC_000017.10:g.8191972A>G , CM000679.1:g.8191972A>G GRCh37
NC_000017.9:g.8132697A>G NCBI36
NG_028189.1:g.5004A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000226105.10:c.-135A>G (RANGRF) ENSP00000226105.6:n.-135A>G
ENST00000380067.6:c.*962T>C (SLC25A35) ENSP00000369407.2:n.*962T>C
ENST00000407006.8:c.-135A>G (RANGRF) ENSP00000383940.4:n.-135A>G
ENST00000579192.5:c.*43-222T>C (SLC25A35) ENSP00000462395.1:n.*43-222T>C
ENST00000581320.1:n.91-222T>C (SLC25A35)
NM_001177801.1:c.-135A>G (RANGRF) NP_001171272.1:n.-135A>G
NM_001177802.1:c.-135A>G (RANGRF) NP_001171273.1:n.-135A>G
NM_016492.4:c.-135A>G (RANGRF) NP_057576.2:n.-135A>G
NM_201520.1:c.*962T>C (SLC25A35) NP_958928.1:n.*962T>C
XM_005256618.3:c.-135A>G (RANGRF) XP_005256675.1:n.-135A>G
NM_001320871.1:c.*43-222T>C (SLC25A35) NP_001307800.1:n.*43-222T>C
NM_001330127.1:c.-135A>G (RANGRF) NP_001317056.1:n.-135A>G
NM_201520.2:c.*962T>C (SLC25A35) NP_958928.1:n.*962T>C
NM_001320871.2:c.*43-222T>C (SLC25A35) NP_001307800.1:n.*43-222T>C
NM_201520.3:c.*962T>C (SLC25A35) NP_958928.1:n.*962T>C
NR_135483.2:n.2507T>C (SLC25A35)