Canonical Allele Identifier: CA2635993272

Gene: RANGRF SLC25A35

Linked Data

• gnomAD v4: 17-8288598-ACC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8288602_8288603del , CM000679.2:g.8288602_8288603del	GRCh38
NC_000017.10:g.8191920_8191921del , CM000679.1:g.8191920_8191921del	GRCh37
NC_000017.9:g.8132645_8132646del	NCBI36
NG_028189.1:g.4952_4953del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226105.10:c.-187_-186del (RANGRF)	ENSP00000226105.6:n.-187_-186del
ENST00000380067.6:c.*1016_*1017del (SLC25A35)	ENSP00000369407.2:n.*1016_*1017del
ENST00000579192.5:c.*43-168_*43-167del (SLC25A35)	ENSP00000462395.1:n.*43-168_*43-167del
ENST00000581320.1:n.91-168_91-167del (SLC25A35)
NM_201520.1:c.*1016_*1017del (SLC25A35)	NP_958928.1:n.*1016_*1017del
XM_005256618.3:c.-187_-186del (RANGRF)	XP_005256675.1:n.-187_-186del
NM_001320871.1:c.*43-168_*43-167del (SLC25A35)	NP_001307800.1:n.*43-168_*43-167del
NM_001330127.1:c.-187_-186del (RANGRF)	NP_001317056.1:n.-187_-186del
NM_201520.2:c.*1016_*1017del (SLC25A35)	NP_958928.1:n.*1016_*1017del
NM_001320871.2:c.*43-168_*43-167del (SLC25A35)	NP_001307800.1:n.*43-168_*43-167del
NM_201520.3:c.*1016_*1017del (SLC25A35)	NP_958928.1:n.*1016_*1017del
NR_135483.2:n.2561_2562del (SLC25A35)