Canonical Allele Identifier: CA2246233224
Gene: RANGRF HGNC NCBI
SLC25A35 HGNC NCBI

Linked Data

dbSNP Id: rs1990235516

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8288771T>C , CM000679.2:g.8288771T>C GRCh38
NC_000017.10:g.8192089T>C , CM000679.1:g.8192089T>C GRCh37
NC_000017.9:g.8132814T>C NCBI36
NG_028189.1:g.5121T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000226105.11:c.-18T>C (RANGRF) MANE Select ENSP00000226105.6:n.-18T>C
ENST00000226105.10:c.-18T>C (RANGRF) ENSP00000226105.6:n.-18T>C
ENST00000380067.6:c.*845A>G (SLC25A35) ENSP00000369407.2:n.*845A>G
ENST00000407006.8:c.-18T>C (RANGRF) ENSP00000383940.4:n.-18T>C
ENST00000439238.3:c.-18T>C (RANGRF) ENSP00000413190.3:n.-18T>C
ENST00000578849.1:n.73T>C (RANGRF)
ENST00000579192.5:c.*43-339A>G (SLC25A35) ENSP00000462395.1:n.*43-339A>G
ENST00000580434.5:c.-18T>C (RANGRF) ENSP00000462310.1:n.-18T>C
ENST00000581320.1:n.90+175A>G (SLC25A35)
NM_001177801.1:c.-18T>C (RANGRF) NP_001171272.1:n.-18T>C
NM_001177802.1:c.-18T>C (RANGRF) NP_001171273.1:n.-18T>C
NM_016492.4:c.-18T>C (RANGRF) NP_057576.2:n.-18T>C
NM_201520.1:c.*845A>G (SLC25A35) NP_958928.1:n.*845A>G
XM_005256618.3:c.-18T>C (RANGRF) XP_005256675.1:n.-18T>C
NM_001320871.1:c.*43-339A>G (SLC25A35) NP_001307800.1:n.*43-339A>G
NM_001330127.1:c.-18T>C (RANGRF) NP_001317056.1:n.-18T>C
NM_201520.2:c.*845A>G (SLC25A35) NP_958928.1:n.*845A>G
NM_016492.5:c.-18T>C (RANGRF) MANE Select NP_057576.2:n.-18T>C
NM_001177801.2:c.-18T>C (RANGRF) NP_001171272.1:n.-18T>C
NM_001177802.2:c.-18T>C (RANGRF) NP_001171273.1:n.-18T>C
NM_001320871.2:c.*43-339A>G (SLC25A35) NP_001307800.1:n.*43-339A>G
NM_001330127.2:c.-18T>C (RANGRF) NP_001317056.1:n.-18T>C
NM_201520.3:c.*845A>G (SLC25A35) NP_958928.1:n.*845A>G
NR_135483.2:n.2390A>G (SLC25A35)