Canonical Allele Identifier: CA287570464

Gene: RANGRF SLC25A35

Linked Data

• dbSNP Id: rs1009475957
• gnomAD v3: 17-8288578-C-T
• gnomAD v4: 17-8288578-C-T
• MyVariant Identifiers: chr17:g.8191896C>T (hg19) ; chr17:g.8288578C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8288578C>T , CM000679.2:g.8288578C>T	GRCh38
NC_000017.10:g.8191896C>T , CM000679.1:g.8191896C>T	GRCh37
NC_000017.9:g.8132621C>T	NCBI36
NG_028189.1:g.4928C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226105.10:c.-211C>T (RANGRF)	ENSP00000226105.6:n.-211C>T
ENST00000380067.6:c.*1038G>A (SLC25A35)	ENSP00000369407.2:n.*1038G>A
ENST00000579192.5:c.*43-146G>A (SLC25A35)	ENSP00000462395.1:n.*43-146G>A
ENST00000581320.1:n.91-146G>A (SLC25A35)
NM_201520.1:c.*1038G>A (SLC25A35)	NP_958928.1:n.*1038G>A
XM_005256618.3:c.-211C>T (RANGRF)	XP_005256675.1:n.-211C>T
NM_001320871.1:c.*43-146G>A (SLC25A35)	NP_001307800.1:n.*43-146G>A
NM_001330127.1:c.-211C>T (RANGRF)	NP_001317056.1:n.-211C>T
NM_201520.2:c.*1038G>A (SLC25A35)	NP_958928.1:n.*1038G>A
NM_001320871.2:c.*43-146G>A (SLC25A35)	NP_001307800.1:n.*43-146G>A
NM_201520.3:c.*1038G>A (SLC25A35)	NP_958928.1:n.*1038G>A
NR_135483.2:n.2583G>A (SLC25A35)