Canonical Allele Identifier: CA2635993313

Gene: RANGRF SLC25A35

Linked Data

• gnomAD v4: 17-8288611-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8288611G>T , CM000679.2:g.8288611G>T	GRCh38
NC_000017.10:g.8191929G>T , CM000679.1:g.8191929G>T	GRCh37
NC_000017.9:g.8132654G>T	NCBI36
NG_028189.1:g.4961G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226105.10:c.-178G>T (RANGRF)	ENSP00000226105.6:n.-178G>T
ENST00000380067.6:c.*1005C>A (SLC25A35)	ENSP00000369407.2:n.*1005C>A
ENST00000579192.5:c.*43-179C>A (SLC25A35)	ENSP00000462395.1:n.*43-179C>A
ENST00000581320.1:n.91-179C>A (SLC25A35)
NM_201520.1:c.*1005C>A (SLC25A35)	NP_958928.1:n.*1005C>A
XM_005256618.3:c.-178G>T (RANGRF)	XP_005256675.1:n.-178G>T
NM_001320871.1:c.*43-179C>A (SLC25A35)	NP_001307800.1:n.*43-179C>A
NM_001330127.1:c.-178G>T (RANGRF)	NP_001317056.1:n.-178G>T
NM_201520.2:c.*1005C>A (SLC25A35)	NP_958928.1:n.*1005C>A
NM_001320871.2:c.*43-179C>A (SLC25A35)	NP_001307800.1:n.*43-179C>A
NM_201520.3:c.*1005C>A (SLC25A35)	NP_958928.1:n.*1005C>A
NR_135483.2:n.2550C>A (SLC25A35)