Canonical Allele Identifier: CA2635993484

Gene: RANGRF SLC25A35

Linked Data

• gnomAD v4: 17-8288683-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8288683G>T , CM000679.2:g.8288683G>T	GRCh38
NC_000017.10:g.8192001G>T , CM000679.1:g.8192001G>T	GRCh37
NC_000017.9:g.8132726G>T	NCBI36
NG_028189.1:g.5033G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226105.11:c.-106G>T (RANGRF) MANE Select	ENSP00000226105.6:n.-106G>T
ENST00000226105.10:c.-106G>T (RANGRF)	ENSP00000226105.6:n.-106G>T
ENST00000380067.6:c.*933C>A (SLC25A35)	ENSP00000369407.2:n.*933C>A
ENST00000407006.8:c.-106G>T (RANGRF)	ENSP00000383940.4:n.-106G>T
ENST00000439238.3:c.-106G>T (RANGRF)	ENSP00000413190.3:n.-106G>T
ENST00000579192.5:c.*43-251C>A (SLC25A35)	ENSP00000462395.1:n.*43-251C>A
ENST00000580434.5:c.-106G>T (RANGRF)	ENSP00000462310.1:n.-106G>T
ENST00000581320.1:n.91-251C>A (SLC25A35)
NM_001177801.1:c.-106G>T (RANGRF)	NP_001171272.1:n.-106G>T
NM_001177802.1:c.-106G>T (RANGRF)	NP_001171273.1:n.-106G>T
NM_016492.4:c.-106G>T (RANGRF)	NP_057576.2:n.-106G>T
NM_201520.1:c.*933C>A (SLC25A35)	NP_958928.1:n.*933C>A
XM_005256618.3:c.-106G>T (RANGRF)	XP_005256675.1:n.-106G>T
NM_001320871.1:c.*43-251C>A (SLC25A35)	NP_001307800.1:n.*43-251C>A
NM_001330127.1:c.-106G>T (RANGRF)	NP_001317056.1:n.-106G>T
NM_201520.2:c.*933C>A (SLC25A35)	NP_958928.1:n.*933C>A
NM_016492.5:c.-106G>T (RANGRF) MANE Select	NP_057576.2:n.-106G>T
NM_001177801.2:c.-106G>T (RANGRF)	NP_001171272.1:n.-106G>T
NM_001177802.2:c.-106G>T (RANGRF)	NP_001171273.1:n.-106G>T
NM_001320871.2:c.*43-251C>A (SLC25A35)	NP_001307800.1:n.*43-251C>A
NM_001330127.2:c.-106G>T (RANGRF)	NP_001317056.1:n.-106G>T
NM_201520.3:c.*933C>A (SLC25A35)	NP_958928.1:n.*933C>A
NR_135483.2:n.2478C>A (SLC25A35)