Canonical Allele Identifier: CA2246233070
Gene: RANGRF HGNC NCBI
SLC25A35 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8288608C= , CM000679.2:g.8288608C= GRCh38
NC_000017.10:g.8191926C= , CM000679.1:g.8191926C= GRCh37
NC_000017.9:g.8132651C= NCBI36
NG_028189.1:g.4958C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000226105.10:c.-181C= (RANGRF) ENSP00000226105.6:n.-181C=
ENST00000380067.6:c.*1008G= (SLC25A35) ENSP00000369407.2:n.*1008G=
ENST00000579192.5:c.*43-176G= (SLC25A35) ENSP00000462395.1:n.*43-176G=
ENST00000581320.1:n.91-176G= (SLC25A35)
NM_201520.1:c.*1008G= (SLC25A35) NP_958928.1:n.*1008G=
XM_005256618.3:c.-181C= (RANGRF) XP_005256675.1:n.-181C=
NM_001320871.1:c.*43-176G= (SLC25A35) NP_001307800.1:n.*43-176G=
NM_001330127.1:c.-181C= (RANGRF) NP_001317056.1:n.-181C=
NM_201520.2:c.*1008G= (SLC25A35) NP_958928.1:n.*1008G=
NM_001320871.2:c.*43-176G= (SLC25A35) NP_001307800.1:n.*43-176G=
NM_201520.3:c.*1008G= (SLC25A35) NP_958928.1:n.*1008G=
NR_135483.2:n.2553G= (SLC25A35)