Canonical Allele Identifier: CA2246233078
Gene: RANGRF HGNC NCBI
SLC25A35 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8288615C= , CM000679.2:g.8288615C= GRCh38
NC_000017.10:g.8191933C= , CM000679.1:g.8191933C= GRCh37
NC_000017.9:g.8132658C= NCBI36
NG_028189.1:g.4965C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000226105.10:c.-174C= (RANGRF) ENSP00000226105.6:n.-174C=
ENST00000380067.6:c.*1001G= (SLC25A35) ENSP00000369407.2:n.*1001G=
ENST00000579192.5:c.*43-183G= (SLC25A35) ENSP00000462395.1:n.*43-183G=
ENST00000581320.1:n.91-183G= (SLC25A35)
NM_201520.1:c.*1001G= (SLC25A35) NP_958928.1:n.*1001G=
XM_005256618.3:c.-174C= (RANGRF) XP_005256675.1:n.-174C=
NM_001320871.1:c.*43-183G= (SLC25A35) NP_001307800.1:n.*43-183G=
NM_001330127.1:c.-174C= (RANGRF) NP_001317056.1:n.-174C=
NM_201520.2:c.*1001G= (SLC25A35) NP_958928.1:n.*1001G=
NM_001320871.2:c.*43-183G= (SLC25A35) NP_001307800.1:n.*43-183G=
NM_201520.3:c.*1001G= (SLC25A35) NP_958928.1:n.*1001G=
NR_135483.2:n.2546G= (SLC25A35)