Canonical Allele Identifier: CA2635993266

Gene: RANGRF SLC25A35

Linked Data

• gnomAD v4: 17-8288598-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8288598A>C , CM000679.2:g.8288598A>C	GRCh38
NC_000017.10:g.8191916A>C , CM000679.1:g.8191916A>C	GRCh37
NC_000017.9:g.8132641A>C	NCBI36
NG_028189.1:g.4948A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226105.10:c.-191A>C (RANGRF)	ENSP00000226105.6:n.-191A>C
ENST00000380067.6:c.*1018T>G (SLC25A35)	ENSP00000369407.2:n.*1018T>G
ENST00000579192.5:c.*43-166T>G (SLC25A35)	ENSP00000462395.1:n.*43-166T>G
ENST00000581320.1:n.91-166T>G (SLC25A35)
NM_201520.1:c.*1018T>G (SLC25A35)	NP_958928.1:n.*1018T>G
XM_005256618.3:c.-191A>C (RANGRF)	XP_005256675.1:n.-191A>C
NM_001320871.1:c.*43-166T>G (SLC25A35)	NP_001307800.1:n.*43-166T>G
NM_001330127.1:c.-191A>C (RANGRF)	NP_001317056.1:n.-191A>C
NM_201520.2:c.*1018T>G (SLC25A35)	NP_958928.1:n.*1018T>G
NM_001320871.2:c.*43-166T>G (SLC25A35)	NP_001307800.1:n.*43-166T>G
NM_201520.3:c.*1018T>G (SLC25A35)	NP_958928.1:n.*1018T>G
NR_135483.2:n.2563T>G (SLC25A35)