Canonical Allele Identifier: CA2635993333

Gene: RANGRF SLC25A35

Linked Data

• gnomAD v4: 17-8288623-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8288623C>A , CM000679.2:g.8288623C>A	GRCh38
NC_000017.10:g.8191941C>A , CM000679.1:g.8191941C>A	GRCh37
NC_000017.9:g.8132666C>A	NCBI36
NG_028189.1:g.4973C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226105.10:c.-166C>A (RANGRF)	ENSP00000226105.6:n.-166C>A
ENST00000380067.6:c.*993G>T (SLC25A35)	ENSP00000369407.2:n.*993G>T
ENST00000579192.5:c.*43-191G>T (SLC25A35)	ENSP00000462395.1:n.*43-191G>T
ENST00000581320.1:n.91-191G>T (SLC25A35)
NM_201520.1:c.*993G>T (SLC25A35)	NP_958928.1:n.*993G>T
XM_005256618.3:c.-166C>A (RANGRF)	XP_005256675.1:n.-166C>A
NM_001320871.1:c.*43-191G>T (SLC25A35)	NP_001307800.1:n.*43-191G>T
NM_001330127.1:c.-166C>A (RANGRF)	NP_001317056.1:n.-166C>A
NM_201520.2:c.*993G>T (SLC25A35)	NP_958928.1:n.*993G>T
NM_001320871.2:c.*43-191G>T (SLC25A35)	NP_001307800.1:n.*43-191G>T
NM_201520.3:c.*993G>T (SLC25A35)	NP_958928.1:n.*993G>T
NR_135483.2:n.2538G>T (SLC25A35)