Canonical Allele Identifier: CA287553705

Gene: RANGRF SLC25A35

Linked Data

• dbSNP Id: rs1007767651
• gnomAD v3: 17-8288639-G-C
• gnomAD v4: 17-8288639-G-C
• MyVariant Identifiers: chr17:g.8191957G>C (hg19) ; chr17:g.8288639G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8288639G>C , CM000679.2:g.8288639G>C	GRCh38
NC_000017.10:g.8191957G>C , CM000679.1:g.8191957G>C	GRCh37
NC_000017.9:g.8132682G>C	NCBI36
NG_028189.1:g.4989G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226105.10:c.-150G>C (RANGRF)	ENSP00000226105.6:n.-150G>C
ENST00000380067.6:c.*977C>G (SLC25A35)	ENSP00000369407.2:n.*977C>G
ENST00000579192.5:c.*43-207C>G (SLC25A35)	ENSP00000462395.1:n.*43-207C>G
ENST00000581320.1:n.91-207C>G (SLC25A35)
NM_201520.1:c.*977C>G (SLC25A35)	NP_958928.1:n.*977C>G
XM_005256618.3:c.-150G>C (RANGRF)	XP_005256675.1:n.-150G>C
NM_001320871.1:c.*43-207C>G (SLC25A35)	NP_001307800.1:n.*43-207C>G
NM_001330127.1:c.-150G>C (RANGRF)	NP_001317056.1:n.-150G>C
NM_201520.2:c.*977C>G (SLC25A35)	NP_958928.1:n.*977C>G
NM_001320871.2:c.*43-207C>G (SLC25A35)	NP_001307800.1:n.*43-207C>G
NM_201520.3:c.*977C>G (SLC25A35)	NP_958928.1:n.*977C>G
NR_135483.2:n.2522C>G (SLC25A35)