Canonical Allele Identifier: CA2635993310

Gene: RANGRF SLC25A35

Linked Data

• gnomAD v4: 17-8288610-AGGGTCTT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8288613_8288619del , CM000679.2:g.8288613_8288619del	GRCh38
NC_000017.10:g.8191931_8191937del , CM000679.1:g.8191931_8191937del	GRCh37
NC_000017.9:g.8132656_8132662del	NCBI36
NG_028189.1:g.4963_4969del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226105.10:c.-176_-170del (RANGRF)	ENSP00000226105.6:n.-176_-170del
ENST00000380067.6:c.*999_*1005del (SLC25A35)	ENSP00000369407.2:n.*999_*1005del
ENST00000579192.5:c.*43-185_*43-179del (SLC25A35)	ENSP00000462395.1:n.*43-185_*43-179del
ENST00000581320.1:n.91-185_91-179del (SLC25A35)
NM_201520.1:c.*999_*1005del (SLC25A35)	NP_958928.1:n.*999_*1005del
XM_005256618.3:c.-176_-170del (RANGRF)	XP_005256675.1:n.-176_-170del
NM_001320871.1:c.*43-185_*43-179del (SLC25A35)	NP_001307800.1:n.*43-185_*43-179del
NM_001330127.1:c.-176_-170del (RANGRF)	NP_001317056.1:n.-176_-170del
NM_201520.2:c.*999_*1005del (SLC25A35)	NP_958928.1:n.*999_*1005del
NM_001320871.2:c.*43-185_*43-179del (SLC25A35)	NP_001307800.1:n.*43-185_*43-179del
NM_201520.3:c.*999_*1005del (SLC25A35)	NP_958928.1:n.*999_*1005del
NR_135483.2:n.2544_2550del (SLC25A35)