Canonical Allele Identifier: CA2635993248

Gene: RANGRF SLC25A35

Linked Data

• gnomAD v4: 17-8288593-C-G

Genomic Alleles

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

Transcript Alleles

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