Canonical Allele Identifier: CA287553677

Gene: RANGRF SLC25A35

Linked Data

• dbSNP Id: rs933101378
• gnomAD v2: 17-8191922-G-A
• gnomAD v4: 17-8288604-G-A
• MyVariant Identifiers: chr17:g.8191922G>A (hg19) ; chr17:g.8288604G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8288604G>A , CM000679.2:g.8288604G>A	GRCh38
NC_000017.10:g.8191922G>A , CM000679.1:g.8191922G>A	GRCh37
NC_000017.9:g.8132647G>A	NCBI36
NG_028189.1:g.4954G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226105.10:c.-185G>A (RANGRF)	ENSP00000226105.6:n.-185G>A
ENST00000380067.6:c.*1012C>T (SLC25A35)	ENSP00000369407.2:n.*1012C>T
ENST00000579192.5:c.*43-172C>T (SLC25A35)	ENSP00000462395.1:n.*43-172C>T
ENST00000581320.1:n.91-172C>T (SLC25A35)
NM_201520.1:c.*1012C>T (SLC25A35)	NP_958928.1:n.*1012C>T
XM_005256618.3:c.-185G>A (RANGRF)	XP_005256675.1:n.-185G>A
NM_001320871.1:c.*43-172C>T (SLC25A35)	NP_001307800.1:n.*43-172C>T
NM_001330127.1:c.-185G>A (RANGRF)	NP_001317056.1:n.-185G>A
NM_201520.2:c.*1012C>T (SLC25A35)	NP_958928.1:n.*1012C>T
NM_001320871.2:c.*43-172C>T (SLC25A35)	NP_001307800.1:n.*43-172C>T
NM_201520.3:c.*1012C>T (SLC25A35)	NP_958928.1:n.*1012C>T
NR_135483.2:n.2557C>T (SLC25A35)