Canonical Allele Identifier: CA2246233052

Gene: RANGRF SLC25A35

Linked Data

• dbSNP Id: rs1990224552
• gnomAD v4: 17-8288593-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8288593C>T , CM000679.2:g.8288593C>T	GRCh38
NC_000017.10:g.8191911C>T , CM000679.1:g.8191911C>T	GRCh37
NC_000017.9:g.8132636C>T	NCBI36
NG_028189.1:g.4943C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226105.10:c.-196C>T (RANGRF)	ENSP00000226105.6:n.-196C>T
ENST00000380067.6:c.*1023G>A (SLC25A35)	ENSP00000369407.2:n.*1023G>A
ENST00000579192.5:c.*43-161G>A (SLC25A35)	ENSP00000462395.1:n.*43-161G>A
ENST00000581320.1:n.91-161G>A (SLC25A35)
NM_201520.1:c.*1023G>A (SLC25A35)	NP_958928.1:n.*1023G>A
XM_005256618.3:c.-196C>T (RANGRF)	XP_005256675.1:n.-196C>T
NM_001320871.1:c.*43-161G>A (SLC25A35)	NP_001307800.1:n.*43-161G>A
NM_001330127.1:c.-196C>T (RANGRF)	NP_001317056.1:n.-196C>T
NM_201520.2:c.*1023G>A (SLC25A35)	NP_958928.1:n.*1023G>A
NM_001320871.2:c.*43-161G>A (SLC25A35)	NP_001307800.1:n.*43-161G>A
NM_201520.3:c.*1023G>A (SLC25A35)	NP_958928.1:n.*1023G>A
NR_135483.2:n.2568G>A (SLC25A35)